نتایج جستجو برای: robinow syndrome

تعداد نتایج: 621936  

2015
Cristalle Soman Ashok Lingappa

Robinow syndrome is an extremely rare genetic disorder. Short-limbed dwarfism, abnormalities in the head, face, and external genitalia, as well as vertebral defects comprise its distinct features. This disorder exists in dominant and recessive patterns. Patients with the dominant pattern exhibit moderate symptoms. More physical characteristics and skeletal abnormalities characterize the recessi...

Journal: :thrita 0
zohreh kavehmanesh department of pediatrics, faculty of medicine, baqiyatallah university of medical sciences, tehran, iran ali reza shafiee student research committee, baqiyatallah university of medical sciences, tehran, ir iran; student research committee, baqiyatallah hospital, molasadra street, vanak place, tehran, ir iran. tel: +98-9192525889, fax: +98-2181264354

introduction robinow syndrome (rs) is an infrequent genetic condition that is characterized by a dysmorphic face, dental anomaly, short stature, mesomelic limb shortening, hand and foot anomalies, and hypoplastic genitalia. the robinow syndrome has been reported from the arab countries and other asian countries, but has not been reported in iranian population so far. case presentation a new bor...

Journal: :Journal of medical genetics 1997
M A Sabry E A Ismail R L al-Naggar N A al-Torki S Farah S A al-Awadi D Obenbergerova L Bastaki

We report on some members of two unrelated families showing the characteristic features of Robinow syndrome. In a consanguineous Kuwaiti family, the index case with Robinow syndrome showed some unusual features including severe IUGR, laxity of ligaments, hyperextensible joints, redundant skin folds, severe normocytic anaemia, repeated infection, increased percentage of total T cells and CD4 pos...

Journal: :American journal of human genetics 2016
Janson J White Juliana F Mazzeu Alexander Hoischen Yavuz Bayram Marjorie Withers Alper Gezdirici Virginia Kimonis Marloes Steehouwer Shalini N Jhangiani Donna M Muzny Richard A Gibbs Bregje W M van Bon V Reid Sutton James R Lupski Han G Brunner Claudia M B Carvalho

Robinow syndrome is a rare congenital disorder characterized by mesomelic limb shortening, genital hypoplasia, and distinctive facial features. Recent reports have identified, in individuals with dominant Robinow syndrome, a specific type of variant characterized by being uniformly located in the penultimate exon of DVL1 and resulting in a -1 frameshift allele with a premature termination codon...

Journal: :European journal of paediatric dentistry : official journal of European Academy of Paediatric Dentistry 2009
N Eronat D Cogulu F Ozkinay

BACKGROUND Robinow syndrome or "foetal face" syndrome is an extremely rare genetic disorder with characteristic skeletal and orofacial findings. The purpose of the present case report is to describe the clinical findings of an 8 year-old female patient with autosomal recessive Robinow syndrome. CASE REPORT The patient was born to consanguineous parents and had anomalies typical of the recessi...

Journal: :Indian Journal of Orthopaedics 2008

Journal: :JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH 2015

Journal: :Turkiye Klinikleri Journal of Dental Sciences 2020

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