Literature DB >> 12002153

An autosomal recessive syndrome of choanal atresia, hypothelia/athelia and thyroid gland anomalies overlapping bamforth syndrome, ANOTHER syndrome and methimazole embryopathy.

L I Al-Gazali1, Z Hamid, J Hertecant, M Bakir, D Nath, A Kakadekar.   

Abstract

Two sibs from an inbred Arab family are described with an autosomal syndrome of choanal atresia, hypothelia/athelia and thyroid gland anomalies overlapping Bamforth syndrome, ANOTHER syndrome and methimazole embryopathy. In one case the syndrome described was lethal. Cases with similar features are reviewed and genetic mutations discussed.

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Year:  2002        PMID: 12002153     DOI: 10.1097/00019605-200204000-00001

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN: 0962-8827            Impact factor:   0.816


  1 in total

1.  Phenotypic expansion of KMT2D-related disorder: Beyond Kabuki syndrome.

Authors:  Dustin Baldridge; Rebecca C Spillmann; Daniel J Wegner; Jennifer A Wambach; Frances V White; Kathleen Sisco; Tomi L Toler; Patricia I Dickson; F Sessions Cole; Vandana Shashi; Dorothy K Grange
Journal:  Am J Med Genet A       Date:  2020-02-21       Impact factor: 2.802

  1 in total

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