Home

Proteus syndrome

Proteus syndrome Genetic and Rare Diseases Information

Proteus syndrome is characterized by excessive growth of a part or portion of the body. The overgrowth is usually asymmetric, which means it affects the right and left sides of the body differently. Newborns with Proteus syndrome have few or no signs of the disorder Clinical characteristics: Proteus syndrome is characterized by progressive segmental or patchy overgrowth most commonly affecting the skeleton, skin, adipose, and central nervous systems. In most individuals Proteus syndrome has modest or no manifestations at birth, develops and progresses rapidly beginning in the toddler period, and relentlessly progresses through childhood, causing severe overgrowth and disfigurement Proteus syndrome is a rare condition characterized by overgrowth of the bones, skin, and other tissues. Organs and tissues affected by the disease grow out of proportion to the rest of the body. The overgrowth is usually asymmetric, which means it affects the right and left sides of the body differently

Proteus syndrome is a rare disorder characterized by overgrowth of various tissues of the body. The cause of the disorder is a mosaic variant in a gene called AKT1. Disproportionate, asymmetric overgrowth occurs in a mosaic pattern (i.e., a random patchy pattern of affected and unaffected areas) متلازمة بروتيوس أو متلازمة وايدمان (سميت نسبة إلى طبيب الأطفال الألماني هانز-رودولف وايدمان) أو متلازمة المتقلبة إغلاق </ref> مفقود لوسم <ref> </ref> أو ظاهرة أعراض البروتيوس (بالإنجليزية: Proteus Syndrome), ويطلق عليه أيضا اسم مرض فيدمان. هو مرض جيني جد معقد يصيب واحد أو عدة مناطق من الجسم. The syndromatic constellation of palmoplantar overgrowth, multiple lipomas, giant fingers and toes, limb overgrowth, venous-lymphatic malformation and a café-au-lait spot led to the diagnosis of Proteus syndrome. The possible aetiology, clinical manifestations, differential diagnosis and management of this rare disorder are discussed Proteus Syndrome is a condition which involves atypical growth of the bones, skin and head, and can lead to a variety of other symptoms. The condition is caused by a genetic mutation in AKT1, an important gene that helps to regulate the growth of cells. Now that genetic testing for the AKT1 mutation is available, it is important to get tested

Proteus syndrome is a rare condition that can be loosely categorized as a hamartomatous disorder. It is a complex disorder with multisystem involvement and great clinical variability Proteus syndrome is an extremely rare but chronic, or long-term, condition. It causes an overgrowth of skin, bones, blood vessels, and fatty and connective tissue. These overgrowths usually aren't.. Proteus Syndrome Background. Proteus syndrome is an extremely rare overgrowth syndrome thought to affect fewer than 500 individuals in the developed world. It is characterized by the progressive and abnormal growth of body tissues, including skin, bones, fatty tissues and blood vessels Proteus Syndrome was first described and categorized by Doctor Michael Cohen in 1979 and was named after the Greek god Proteus. This Greek god was capable of changing his shape. This name was chosen to reflect the gradual changes a person when through who was diagnosed with Proteus Syndrome

Proteus Syndrome - PubMe

Proteus syndrome is a rare congenital, multisystemic, hamartomatous condition characterized by asymmetrical overgrowth of almost any part of the body and a broad spectrum of manifestations. It can affect tissue from any germinal layer. It is suspected to be a genetic condition, but a particular gene is not currently identified Subscribe today and give the gift of knowledge to yourself or a friend proteus syndrome Proteus Syndrome. By: Aislin Anderson Leah Oswald. Symptoms. O.. Proteus Syndrome. Proteus syndrome (PS) is a complex hamartomatous disorder consisting of disproportionate, asymmetric overgrowth of any tissue of the body, particularly the skeleton, cerebriform connective tissue nevi, epidermal nevi, vascular malformations, and dysregulated adipose tissue (Cohen, 2005; Biesecker, 2006) Proteus syndrome is a rare disorder that affects the normal growth of the bones progressively. It causes abnormal growth of the skin adipose and central nervous system. The baby with Proteus syndrome would have normal bone growth during birth but when it reaches 1 year or 2 the bones of hands and feet would grow [

Proteus syndrome: MedlinePlus Genetic

  1. Proteus syndrome is a medical condition that leads to disproportionate growth of tissues such as bone, skin, vascular and fatty tissue. This page from Great Ormond Street Hospital (GOSH) explains the causes, symptoms and treatment of Proteus syndrome and where to get help. A syndrome is a collection of signs and symptoms that have the same cause
  2. Proteus syndrome is a rare condition characterized by progressive overgrowth of the bones, skin, adipose tissue and central nervous system 1). Organs and tissues affected by Proteus syndrome grow out of proportion to the rest of the body. The overgrowth is usually asymmetric, which means it affects the right and left sides of the body differently
  3. Proteus syndrome is a highly variable, severe disorder of asymmetric and disproportionate overgrowth of body parts, connective tissue nevi, epidermal nevi, dysregulated adipose tissue, and vascular malformations. Specific features include cerebriform connective tissue nevus, thin limbs, lipomas, and lung cysts
  4. Drug therapy is not currently a component of the standard of care for Proteus syndrome (see Treatment). However, a study by Lindhurst et al indicated that ARQ 092 reduces the abnormally increased..
  5. Proteus syndrome is characterized by progressive segmental or patchy overgrowth most commonly affecting the skeleton, skin, adipose, and central nervous systems. In most individuals Proteus syndrome has modest or no manifestations at birth, develops and progresses rapidly beginning in the toddler period, and relentlessly progresses through childhood, causing severe overgrowth and disfigurement

Proteus Syndrome - NORD (National Organization for Rare

Proteus syndrome is a disorder of segmental or mosaic overgrowth that can affect any tissue. The most common manifestations include overgrowth that can lead to orthopedic complications, soft tissue overgrowth of the feet, linear nevi, vascular malformations, and tumor predisposition Disease definition Proteus syndrome (PS) is a very rare and complex hamartomatous overgrowth disorder characterized by progressive overgrowth of the skeleton, skin, adipose, and central nervous systems Introduction. Proteus syndrome is a rare congenital disorder that produces multifocal overgrowth of tissue. It may affect tissues derived from any of the three germinal layers (, 1 2).As of 1999, fewer than 200 cases of Proteus syndrome had been reported in the literature (, 3), and many of these cases do not meet the currently accepted diagnostic criteria (Biesecker LG, oral communication. Proteus syndrome is an extremely rare genetic condition that causes tissues of the body, such as skin and bone, to overgrow. The overgrowth often happens disproportionately, and can severely change a person's appearance. The condition was named after the Greek god Proteus, who could take on different shapes at will. Verywell/Jessica Olah

Teen with progeria continues to beat staggering odds - YouTube

Proteus syndrome is a rare overgrowth condition. The overgrowth in Proteus syndrome can cause differences in the appearance and growth rate of various body parts. This overgrowth is also typically asymmetric, that is, it does not affect corresponding body parts similarly. The word Proteus comes from the name of the ancient Greek god of change Proteus syndrome was originally described in two patients by Cohen and Hayden [1979] as a newly recognized disorder characterized by overgrowth of multiple tissues, connective tissue nevi, epidermal nevi, and hyperostoses. The disorder was designated Proteus syndrome by Wiedemann et al. [1983] to denote its variability of clinical expression Proteus syndrome is an extremely rare genetic disorder that is characterised by the abnormal growth of bones and blood vessels, and various skin lesions including lipomas, epidermal naevi and café au lait macules. The condition is usually not evident until late infancy or early childhood when signs and symptoms start to appear Proteus syndrome is another form of disease that is rare and congenital in origin. The condition is also referred as Wiedemann's syndrome, coined after Hans-Rudolf Wiedemann. The condition is characterized by the overgrowth of skin and bone development. There is also growth of the body tissues that makes the affected grow in size asymmetrically

Proteus syndrome is a rare condition characterized by progressive overgrowth of the bones, skin, adipose tissue and central nervous system 1). Organs and tissues affected by Proteus syndrome grow out of proportion to the rest of the body. The overgrowth is usually asymmetric, which means it affects the right and left sides of the body differently Proteus syndrome is an uncommon state of abnormal growth. The developmental abnormalities associated with this syndrome can lead to unusual look and overgrowth of different parts of the body. The growth is not symmetric, which means that the parallel parts of the body are not of the corresponding length of the other

PTEN hamartoma tumor syndrome: An overview | Genetics in

Proteus syndrome (PS) was described as a discrete clinical entity in 1979 1 and assigned its name several years later. 2 This is a relatively recently delineated syndrome, probably because it is. Proteus syndrome is a mosaic, progressive overgrowth disorder caused by a somatic activating variant c.49G > A p. (E17K) in AKT1. The presentation in affected individuals is variable, with a diversity of tissues demonstrating abnormalities. Common manifestations include skin and bony overgrowth, vascular malformations (VMs), cysts and benign. Proteus Syndrome. Definition: Proteus Syndrome is a rare genetic disorder, caused by mutant genes. The skin, bone and tissue disorder is asymmetric. The overgrowth is usually asymmetric, which means it affects the right and left sides of the body differently

متلازمة بروتيوس - ويكيبيدي

Proteus syndrome - PubMe

Klippel-Trenaunay-Weber syndrome (KTWS) left leg 34 year

Proteus syndrome (OMIM # 176920) ( OMIM™ 2005 ), a rare and highly variable congenital hamartomatous disorder ( Gorlin et al. 2001 ), is a member of a group designated as local overgrowth diseases ( Cohen et al. 2002 ). It consists of asymmetric (mosaic), disproportionate and progressive overgrowth of body parts, connective tissue. Proteus syndrome is a rare condition that has a variable clinical presentation. The syndrome is characterized by asymmetric disproportionate enlargement of the limbs, skull, or vertebrae, associated with a number of cutaneous lesions. Herein, the clinical findings of 2 patients with Proteus syndrome are presented and the current clinical diagnostic criteria are reviewed Proteus syndrome (PS) is an extremely rare disease characterized by excessive chimeric growth of cells, and progressive and irregular asymmetrical hyperplasia. Herein, a PS case with atypical clinical features and syndromes was reported, to improve the understanding of the diagnosis and treatment of the disease. The case was a 3-year-and-11-month-old male child

Proteus syndrome (PS) is a rare complex disorder that produces a multifocal overgrowth of tissue in multiple systems [1]. The name was coined in 1983 by Wiedemann et al [2] after the Greek mythological god of the sea, Proteus, who was capable of changing his shape and form at will in order to avoid capture Proteus Syndrome. By the time 39-year-old Ricky Watson saw Amber Luong, MD, PhD, FACS, he could no longer swallow, eat or talk. His only avenue of communication with his family was writing on a notepad or texting via cell phone. Diagnosed at the age of 10 with Proteus syndrome, an extremely rare condition marked by overgrowth of bones, skin and. Overview. Proteus syndrome is characterized by excessive growth of a part or portion of the body. The overgrowth is usually asymmetric, which means it affects the right and left sides of the body differently. Newborns with Proteus syndrome have few or no signs of the disorder. Overgrowth becomes apparent between the ages of 6 and 18 months and becomes more severe with age

Proteus Syndrome Foundation - Support and Educatio

Sharma determined that Merrick had Proteus syndrome, an extremely rare disorder, itself only identified in 1979. Proteus Syndrome Named for the Greek god who could change his shape, this rare hereditary disorder is characterized by Proteus Syndrome. Proteus Syndrome is a rare syndrome and is considered a progressive overgrowth syndrome. The overgrowth can involve many different tissues, such as the nervous system, the skin and tissue below the skin, connective tissue and organs. This syndrome is caused by a genetic mutation. Hamartomas (non-cancerous tumor-like growths of. Proteus syndrome is an extremely rare complex disorder characterized by patchy or mosaic postnatal overgrowth of different body parts . Proteus syndrome was first described by Cohen and Hayden in 1979 , with an estimated prevalence of <1/1,000,000 live births (3,4). The onset may involve any site of the body and typically occurs during infancy Proteus syndrome involves atypical growth of the bones, skin, head and a variety of other symptoms. It was first identified by Michael Cohen Jr. in 1979. The name comes from the Greek god Proteus. Proteus syndrome is a rare post-natal overgrowth disorder with asymmetric overgrowth of any body tissue. It has a mosaic distribution, progressive course, and sporadic occurrence 1,2,3.It was.

Proteus syndrome definition at Dictionary.com, a free online dictionary with pronunciation, synonyms and translation. Look it up now Proteus syndrome. Proteus syndrome results from assymetric and patchy overgrowth of various tissues including bones and connective tissues. Most of the time there are no signs at birth. The overgrowth is usually not cancerous but can cause significant medical issues related to function, appearance and compression of blood vessels and organs Proteus syndrome may have distinctive facial features with a long face, low nasal bridge, large nostrils and downturned outer part of the eye. Some children have seizures, vision problems and learning difficulties. How is Proteus syndrome diagnosed? As Proteus syndrome is a rare condition, diagnosis will usually only be possible at a specialist. Proteus syndrome is a rare, congenital, hamartomatous disorder affecting all three germ cell layers and potentially all bodily tissues. It is characterised by disproportionate, asymmetrical overgrowth and skeletal abnormalities which are distorting and relentlessly progressive Proteus syndrome is a genetic condition where patients' organs and tissues grow out of proportion to the rest of the body. The disease usually starts in infancy and can involve any tissue or organ. The overgrowth is usually asymmetric, which means that it affects the right and left sides of the body differently

Proteus syndrome, also called elattoproteus syndrome or elephant man disease, is a rare genetic condition affecting about one in a million people in the world. Proteus syndrome cannot be cured. There are, however, several medical options to manage the signs and symptoms of the condition Het proteussyndroom ofwel syndroom van Proteus, is een (zeer) zeldzame genetische aandoening, waarbij de patiënt lijdt aan overmatige of asymmetrische groei of misvormingen van verschillende typen weefsels, die blijft verergeren.Het syndroom kenmerkt zich doordat het zich moeilijk laat diagnosticeren, omdat de variatie aan verschijnselen in principe bij ieder mens die het heeft verschilt

Modern Day Elephant Man - thehumanmarvels

Proteus Syndrome: Background, Pathophysiology, Epidemiolog

Proteus Syndrome is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings).Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity プロテウス症候群 (プロテウスしょうこうぐん、Proteus syndrome) は遺伝学的背景を持つ希少疾患で 、3つの胚葉の全てで組織の過成長が引き起こされる可能性がある。 プロテウス症候群の患者は、胎児性腫瘍のリスクが増大する傾向がある 。 プロテウス症候群の臨床的・放射線医学的症状は非常. Proteus syndrome gained wide public attention in 1980, through the movie The Elephant Man, about a 19th century Londoner whom experts believe may have suffered from the disease. Researchers found that a point mutation — a single-letter misspelling in the DNA of the genetic code — in the AKT1 gene activates the sporadic tissue growth. Síntomas del síndrome de Proteus. Los síntomas tienden a variar mucho de una persona a otra y pueden incluir: Crecimientos excesivos asimétricos, como que un lado del cuerpo tiene extremidades más largas que el otro. lesiones cutáneas elevadas y ásperas que pueden tener una apariencia irregular y estriada Cohen MM. Proteus Syndrome American Journal of Medical Genetics Part C: Seminars in Medical Genetics 137C(1): 38-52, Luglio 2005. van Aalst JA, Bhuller A, Sadove MA. Pediatric vascular lesions J Craniofacial Surg 14(4):566-583 (2003). Voci correlate. Sindrome CLOVES; Altri progett

Proteus syndrome causes an overgrowth of various tissues, including skin, bones, muscles, fatty tissues, and blood and lymphatic vessels. It is characterized by tumors just beneath the skin, excessive growth of the bone, overgrowth of connective tissue in palms of hands and soles of feet, pigmented birthmarks or moles, and partial gigantism of. اسباب متلازمة بروتيوس Proteus Syndrome وعلاجها. مرض بروتيوس أو ظاهرة أعراض بروتيوس أو مرض فيدمان يعتبر، مرض جيني معقد يصيب منطقة أو أكثر من الجسم كالبشرة،العظام ، النخاع الشوكي. تعتبر متلازمة.

Proteus Syndrome: Symptoms, Treatment, Outlook, and Mor

Proteus Syndrome probably develops when a misprint occurs in a certain genes of a child. Genes are a chemical alphabet stored in the body. Genes contain the body's 'built-in' plan to make sure all the parts of the body grow correctly. If a gene has a misprint in the chemical alphabet then a part of the body may not grow correctly Proteus syndrome is an extremely rare disorder that manifests as an asymmetric, disproportionate overgrowth of any connective tissue, such as bone, fat or epidermal nevi, in a mosaic or patchy pattern. It has an estimated prevalence of less than 1/1,000,000 live births. The diagnosis can be difficult because the phenotypes of the patients are variable Proteus syndrome is a rare and complex condition that involves a number of body systems and varies from one affected person to another. Currently, there are less than 100 cases of confirmed Proteus syndrome in the world Proteus syndrome (PS) is a rare pathology characterized by mosaic and progressive hypertrophies, that can affect any organ or tissue of the body. A genetic mutation in the embryo is at the origin of the disease. Bones, fat, skin and connective tissue are the tissues most typically involved. The extent and severity of the abnormalities vary, giving different clinical presentations Proteus syndrome is a rare syndrome characterized by disproportionate overgrowth of limbs, multiple hamartomas, and vascular malformations. The cerebriform connective tissue nevi, also called cerebriform plantar hyperplasia, are present in most patients, and is the main characteristic of the syndrome. If present, even alone, they can be.

Proteus Syndrome - Background - Genom

Proteus Syndrome By : Makayla Puckhaber, Jenna Henderson, Greta Elkin, and Mario Gonzalez 11 What is the exact name of this disorder?Proteus Disorder @emaze_tweets is the leading online #presentation software proteus syndrome. Ze!Converter - Download Video From Dailymotion to mp4, mp3, aac, m4a, f4v, or 3gp for free! proteus syndrome - this is an unpleasant disease. The photos of proteus syndrome below are not recommended for people with a weak psyche! We wish you a cure and never get sick of this disease Das Proteus-Syndrom ist eine sehr seltene Erkrankung. Weltweit sind etwa nur 100 bis 200 Fälle bekannt. Dabei bewirken genetische Veränderungen, dass manche Gliedmaßen oder Körperpartien der Patienten übermäßig wachsen - beispielsweise die Zehen, ein Arm oder auch eine gesamte Körperhälfte Proteus syndrome is a rare overgrowth condition. The overgrowth in Proteus syndrome can cause differences in the appearance and growth rate of various body parts. This overgrowth is such that it does not affect corresponding body parts similarly. The word Proteus comes from the name of th Proteus syndrome is a rare genetic disorder distinguished by an overgrowth of many different tissues in the body in a mosaic pattern. The skin, the musculoskeletal system, the central nervous system, and adipose tissues are affected the most, producing profound disfigurement and life-threatening complications. The diagnosis is made through a combination of clinical criteria and positive.

Proteus Syndrome - Life Expectancy, Pictures, Treatmen

The congenital hamartomatous syndrome known as the Proteus syndrome (PS) manifests itself with regional giantism, lymphangiomatous hamartomas, and other variable features. Review of the medical literature shows approximately 50 cases reported to date. Since this syndrome has only recently been defined, the management of these patients has. Proteus syndrome- Note the generalized overgrowth, upper and lower limb length discrepancy, localized limb distortion of the left knee (A), postural flexion deformity of the left knee (B), and mild dorsal scoliotic deformity (C). Case courtesy by Tamer Ahmed EL-Sobky Et A Le syndrome de Protée est une maladie génétique complexe comprenant des hamartomes de taille importante impliquant plusieurs tissus : tissu conjonctif, tissu épidermique et tissu osseux. Elle se manifeste dès la naissance et les hamartomes grandissent au cours de la vie. Les tumeurs malignes sont rares. Des tumeurs de l'ovaire, des tumeurs testiculaires, des tumeurs de la parotide et des. Proteus syndrome is a very rare condition with a prevalence less than 1/1,000,000. This is a possible reason why sometimes it can be difficult to differentiate endocrine and genetic pathologies with certainty. References 1 article features images from this case. The proteus syndrome. Partial gigantism of the hands and/or feet, nevi, hemihypertrophy, subcutaneous tumors, macrocephaly or other skull anomalies and possible accelerated growth and visceral affections. H. -R. Wiedemann. 1

Proteus syndrome.5 Attaching even a qualified label of Proteus to such patients is not useful for clinical or scientific purposes. Based on these points, we suggest that a more reasonable conclusion for the work by Zhou and colleagues is that patients with overgrowth syndromes who also. Proteus syndrome is a rare, sporadic, sometimes lethal disorder with progressive asymmetric overgrowth of multiple tissues and a propensity to develop particular neoplasms. 1-7 Skin abnormalities in Proteus syndrome include cerebriform connective tissue nevi, epidermal nevi, vascular malformations, lipomas, lipohypoplasia, and dermal hypoplasia. Proteus syndrome, named after the Greek god Proteus, who changes his shape to elude capture, is a rare disease with only about 500 cases globally Proteus syndrome may be complicated by kidney abnormalities, cystic lung disease, eye disorders such as crossed eyes, tumors, and cysts of the eyeballs. Causes Proteus syndrome is caused by a mutation in a growth regulatory gene called AKT1 that occurs after fertilization of the embryo (somatic mutation) Proteus syndrome: A disturbance of cell growth that causes overgrowth, asymmetry, and gigantism of bones, limbs, skin, and other organs. Its symptoms also include vascular malformations; raised, rough skin; and overgrowth of fat.John Merrick, the 19th-century Englishman known as the 'elephant man,' is thought to have had Proteus syndrome

Proteus syndrome Radiology Reference Article

proteus syndrome - YouTub

20 of the Most Shocking Physical Mutations

Proteus Syndrome/Proteus-like Syndrome. PS/PS-like (PSL) is an extremely rare congenital disorder with generalized, unilateral, or localized hamartomatous overgrowth of any tissue. Unusual malignancies have been observed, such as cystadenoma of the ovary, testicular tumors, central nervous system tumors, and parotid monomorphic adenomas Proteus syndrome Background. Proteus syndrome is a rare disorder named after the Greek god Proteus, 'the polymorphous', who could change shape at will to avoid capture. The name reflects the highly variable presentation of this disorder. Wiedemann and colleagues in 1983 who named it were unaware that this syndrome had already been described Proteus syndrome is a rare disorder with a genetic background that can cause tissue overgrowth involving all three embryonic lineages. Patients with Proteus syndrome tend to have an increased risk of embryonic tumor development. The clinical and radiographic manifestations of Proteus syndrome are highly variable. Yet, the orthopedic manifestations of the syndrome are unique. The syndrome is.

Sonographic Identification of Klippel-Trenaunay-Weber SyndromeProteus mirabilis - Quip Labs10 weird medical conditions that will shock you - ReadNonmelanocytic congenital naevi | DermNet NZ

Proteus syndrome. human disease characterized by an overgrowth of skin, bones, muscles, fatty tissues, and blood and lymphatic vessels. Upload media. Wikipedia. Instance of. head and neck disease, developmental defect during embryogenesis. Subclass of Proteus syndrome synonyms, Proteus syndrome pronunciation, Proteus syndrome translation, English dictionary definition of Proteus syndrome. n pathol a condition caused by malfunction in cell growth, in which bone and flesh tissue overgrow in localized areas of the body Collins English Dictionary.. The Proteus Syndrome report provides an overview of therapeutic pipeline activity and therapeutic assessment of the products by development stage, product type, route of administration, molecule.

  • أسماء تمارين البطن.
  • كلام له معنى في الحياة.
  • تطعيم الهربس للاطفال.
  • Fieming دواء.
  • عملية فتحة في سقف الحلق.
  • خريطة مدن السودان.
  • شكل الأطفال حديثي الولادة.
  • الممثلة زوي.
  • شرائح الشوكولاتة للكوفي.
  • هل الله يعاقب الزاني بعد توبته.
  • خاتمة بحث عن أطفال الشوارع في مصر.
  • موضوع عن الكهرباء.
  • قطعيات اللحوم بالانجليزي.
  • الفرق بين الألماس والزركون.
  • زواج باريش أردوتش.
  • دواء للبرد سريع المفعول.
  • مدرسة الخلاعة pdf.
  • الغوص تحت الماء بالانجليزي.
  • قصة حب تاج محل.
  • كريم رتن اي للتصبغات.
  • حكم التصوير الفوتوغرافي للذكرى.
  • قناة فريدة توك.
  • افطار صائم جمعية رسالة.
  • حقائق عن الرجل.
  • تعريف الدم لغة واصطلاحا.
  • ألواح أكريليك الكويت.
  • مدة سجن السارق في السعودية.
  • موضوع عن الخبز.
  • أعراض السحر المأكول القديم.
  • خلوص الشنبر.
  • هل البنك يسأل عن مصدر الفلوس.
  • علم الآلات الموسيقية.
  • ماذا نقول عند غسل الحيض.
  • إنجلترا أين تقع.
  • مدن إيطاليا تستحق الزيارة.
  • ماهي مشاكل الخادمات الاثيوبيات.
  • ريديتش.
  • حذاء جلد نسائي.
  • تعريف الدم لغة واصطلاحا.
  • تنزيل متصفح سريع وحديث.
  • أهمية التوعية الصحية.