Literature DB >> 9375925

Congenital glaucoma, limb deformities, skeletal dysplasia, and facial anomalies: report of another family.

A Mégarbané1, K Tomey, G Wakim.   

Abstract

We report on a family of first cousin parents in which 2 of 3 children presented with congenital glaucoma, large anterior fontanelle, prominent forehead, hypertelorism, down-slanting palpebral fissures, broad and flat nasal bridge, broad nasal tip, anteverted nostrils, high-arched palate, gingival hypertrophy, pectus excavatum, prominent coccyx with skin fold, short fingers and toes, single palmar creases, flexion deformities of fingers, club feet, and osseous malformations. Despite some clinical differences, their anomalies are very similar to those seen in a new and rare autosomal recessive entity described by ter Haar et al. [1982]. Differential diagnoses are discussed.

Entities:  

Mesh:

Year:  1997        PMID: 9375925     DOI: 10.1002/(sici)1096-8628(19971128)73:1<67::aid-ajmg13>3.0.co;2-p

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  6 in total

Review 1.  Frank-Ter Haar syndrome in a newborn.

Authors:  P Femitha; Rojo Joy; Bahubali D Gane; B Adhisivam; B Vishnu Bhat
Journal:  Indian J Pediatr       Date:  2011-10-29       Impact factor: 1.967

2.  A review of the diverse genetic disorders in the Lebanese population: highlighting the urgency for community genetic services.

Authors:  Ghunwa Nakouzi; Khalil Kreidieh; Soha Yazbek
Journal:  J Community Genet       Date:  2014-09-27

3.  Disruption of the podosome adaptor protein TKS4 (SH3PXD2B) causes the skeletal dysplasia, eye, and cardiac abnormalities of Frank-Ter Haar Syndrome.

Authors:  Zafar Iqbal; Pilar Cejudo-Martin; Arjan de Brouwer; Bert van der Zwaag; Pilar Ruiz-Lozano; M Cecilia Scimia; James D Lindsey; Robert Weinreb; Beate Albrecht; Andre Megarbane; Yasemin Alanay; Ziva Ben-Neriah; Mariangela Amenduni; Rosangela Artuso; Joris A Veltman; Ellen van Beusekom; Astrid Oudakker; José Luis Millán; Raoul Hennekam; Ben Hamel; Sara A Courtneidge; Hans van Bokhoven
Journal:  Am J Hum Genet       Date:  2010-02-04       Impact factor: 11.025

4.  The novel zebrafish model pretzel demonstrates a central role for SH3PXD2B in defective collagen remodelling and fibrosis in Frank-Ter Haar syndrome.

Authors:  Ivo J H M de Vos; Arnette Shi Wei Wong; Jason Taslim; Sheena Li Ming Ong; Nicole C Syder; Julian L Goggi; Thomas J Carney; Maurice A M van Steensel
Journal:  Biol Open       Date:  2020-12-29       Impact factor: 2.422

5.  The Role of the Disrupted Podosome Adaptor Protein (SH3PXD2B) in Frank-Ter Haar Syndrome.

Authors:  Salam Massadeh; Fahad Alhabshan; Hadeel N AlSudairi; Sarah Alkwai; Moneera Alsuwailm; Mohamed S Kabbani; Farah Chaikhouni; Manal Alaamery
Journal:  Genes (Basel)       Date:  2022-01-27       Impact factor: 4.096

6.  Mutations in SH3PXD2B cause Borrone dermato-cardio-skeletal syndrome.

Authors:  Gabrielle R Wilson; Jasmine Sunley; Katherine R Smith; Kate Pope; Catherine J Bromhead; Elizabeth Fitzpatrick; Maja Di Rocco; Maurice van Steensel; David J Coman; Richard J Leventer; Martin B Delatycki; David J Amor; Melanie Bahlo; Paul J Lockhart
Journal:  Eur J Hum Genet       Date:  2013-10-09       Impact factor: 4.246

  6 in total

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