نتایج جستجو برای: robinow syndrome

تعداد نتایج: 621936  

Journal: :Rio de Janeiro Dental Journal (Revista Científica do CRO-RJ) 2019

2014
Chunqiao Liu Chen Lin Chun Gao Helen May-Simera Anand Swaroop Tiansen Li

Planar cell polarity (PCP) signaling plays a critical role in tissue morphogenesis. In mammals, disruption of three of the six "core PCP" components results in polarity-dependent defects with rotated cochlear hair cell stereocilia and open neural tube. We recently demonstrated a role of Prickle1, a core PCP molecule in Drosophila, in mammalian neuronal development. To examine Prickle1 function ...

Journal: :Clinical genetics 2010
J F Mazzeu A M Vianna-Morgante A C V Krepischi A Oudakker C Rosenberg K Szuhai J McGill J Maccraughan H van Bokhoven H G Brunner

To the Editor : Microdeletions at 1q41q42.1 have been described in patients with a variable phenotype that in some cases is suggestive of Fryns syndrome (FS) (1). We have described a similar microdeletion (2) in a boy (hereafter named Patient 1) with clinical features of the dominant form of Robinow syndrome (DRS; 3–5). Here, we report a girl (Patient 2; Fig1a-c) diagnosed as having DRS based o...

2018
Aida M. Mossaad Moustapha A. Abdelrahman Mostafa A. Ibrahim Hatem H. Al Ahmady

BACKGROUND Robinow Syndrome is an extremely rare genetic disorder characterised by abnormalities in head, face and external genitalia. This disorder exists in dominant pattern with moderate symptoms and recessive pattern with more physical and skeletal abnormalities. It was first introduced by Menihard Robinow in 1969. It was related to chromosome 9q22 ROR2 gene related to bone and cartilage gr...

Journal: :The Journal of Korea Assosiation for Disability and Oral Health 2016

2017
Bolette F. Jeppesen Hanne B. Hove Sven Kreiborg Nuno V. Hermann Tron A. Darvann Finn Stener Jørgensen

This article hypothesizes that it is possible to detect and diagnose both the autosomal recessive and dominant forms prenatally using ultrasound. By focusing on the characteristic phenotypical presentation, the examinator is able to diagnose the syndrome prenatally, which is of clinical importance to the parents and counseling for the consideration of terminating the pregnancy.

2016
Shruti Saraswat Satish Mohanty

Abstract Background Robinow syndrome is a rare congenital disorder with phenotypically heterogeneous abnormalities. Two modes of inheritances are known for this syndrome namely autosomal recessive and autosomal dominant. Case Report We describe here an eighteen-month-old child who had mesomelic short stature, abnormal facial features, clinodactyly, micropenis and vertebral changes which were fu...

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