Literature DB >> 1633641

Mental retardation with blepharo-naso-facial abnormalities and hand malformations: a new syndrome?

L van Maldergem1, C Wetzburger, A Verloes, C Fourneau, Y Gillerot.   

Abstract

A syndrome involving facial abnormalities (telecanthus, epicanthus, broad flattened nose, large inverted W-shaped mouth and malformed ears), malformed extremities (camptodactyly, clinodactyly, interdigital webbing and joint hyperlaxity) and mental retardation is described in a girl at birth and at 11 years old. A comparison with Pashayan-Pruzansky syndrome, fetal alcohol syndrome, VATER association, Marden-Walker syndrome and Tel-Hashomer syndrome is discussed. We suggest this patient represents a new malformation syndrome or an extreme phenotypic variant of one of the above-mentioned syndromes.

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Year:  1992        PMID: 1633641     DOI: 10.1111/j.1399-0004.1992.tb03622.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  7 in total

1.  Van Maldergem syndrome: further characterisation and evidence for neuronal migration abnormalities and autosomal recessive inheritance.

Authors:  Sahar Mansour; Marielle Swinkels; Paulien A Terhal; Louise C Wilson; Philip Rich; Lionel Van Maldergem; Petra J G Zwijnenburg; Christine M Hall; Stephen P Robertson; Ruth Newbury-Ecob
Journal:  Eur J Hum Genet       Date:  2012-04-04       Impact factor: 4.246

2.  Whole-Exome Sequencing Reveals FAT4 Mutations in a Clinically Unrecognizable Patient with Syndromic CAKUT: A Case Report.

Authors:  Amelie T van der Ven; Shirlee Shril; Hadas Ityel; Asaf Vivante; Jing Chen; Daw-Yang Hwang; Kristen M Laricchia; Monkol Lek; Velibor Tasic; Friedhelm Hildebrandt
Journal:  Mol Syndromol       Date:  2017-07-01

3.  Hennekam syndrome can be caused by FAT4 mutations and be allelic to Van Maldergem syndrome.

Authors:  Mariëlle Alders; Lihadh Al-Gazali; Isabelle Cordeiro; Bruno Dallapiccola; Livia Garavelli; Beyhan Tuysuz; Faranak Salehi; Martin A Haagmans; Olaf R Mook; Charles B Majoie; Marcel M Mannens; Raoul C Hennekam
Journal:  Hum Genet       Date:  2014-06-07       Impact factor: 4.132

4.  Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development.

Authors:  Silvia Cappello; Mary J Gray; Caroline Badouel; Simona Lange; Melanie Einsiedler; Myriam Srour; David Chitayat; Fadi F Hamdan; Zandra A Jenkins; Tim Morgan; Nadia Preitner; Tami Uster; Jackie Thomas; Patrick Shannon; Victoria Morrison; Nataliya Di Donato; Lionel Van Maldergem; Teresa Neuhann; Ruth Newbury-Ecob; Marielle Swinkells; Paulien Terhal; Louise C Wilson; Petra J G Zwijnenburg; Andrew J Sutherland-Smith; Michael A Black; David Markie; Jacques L Michaud; Michael A Simpson; Sahar Mansour; Helen McNeill; Magdalena Götz; Stephen P Robertson
Journal:  Nat Genet       Date:  2013-09-22       Impact factor: 38.330

5.  A patient with van Maldergem syndrome with endocrine abnormalities, hypogonadotropic hypogonadism, and breast aplasia/hypoplasia.

Authors:  Juan Sotos; Katherine Miller; Donald Corsmeier; Naomi Tokar; Benjamin Kelly; Vijay Nadella; Huachun Zhong; Amy Wetzel; Brent Adler; Chack-Yung Yu; Peter White
Journal:  Int J Pediatr Endocrinol       Date:  2017-10-13

6.  Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants.

Authors:  Islam Oguz Tuncay; Nancy L Parmalee; Raida Khalil; Kiran Kaur; Ashwani Kumar; Mohamed Jimale; Jennifer L Howe; Kimberly Goodspeed; Patricia Evans; Loai Alzghoul; Chao Xing; Stephen W Scherer; Maria H Chahrour
Journal:  NPJ Genom Med       Date:  2022-02-21       Impact factor: 8.617

7.  Requirement of FAT and DCHS protocadherins during hypothalamic-pituitary development.

Authors:  Emily J Lodge; Paraskevi Xekouki; Tatiane S Silva; Cristiane Kochi; Carlos A Longui; Fabio R Faucz; Alice Santambrogio; James L Mills; Nathan Pankratz; John Lane; Dominika Sosnowska; Tina Hodgson; Amanda L Patist; Philippa Francis-West; Francoise Helmbacher; Constantine Stratakis; Cynthia L Andoniadou
Journal:  JCI Insight       Date:  2020-10-27
  7 in total

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