Literature DB >> 12548738

A new autosomal recessive congenital contractural syndrome in an Israeli Bedouin kindred.

Daniella Landau1, Anat Mishori-Dery, Reli Hershkovitz, Ginat Narkis, Khalil Elbedour, Rivka Carmi.   

Abstract

We describe 23 cases with a syndrome of congenital contractures belonging to a large, inbred Israeli-Bedouin kindred. The phenotype described is similar to the Finnish type lethal congenital contracture syndrome yet differs in the following ways: by some additional craniofacial/ocular findings, by the lack of hydrops, multiple pterygia, and fractures, and by the normal duration of pregnancy. The major unique and previously undescribed clinical feature in our patients is a markedly distended urinary bladder as well as other urinary abnormalities. The vast majority of the cases died shortly after birth. Sonographic prenatal diagnosis was possible as early as 15 weeks gestation by demonstrating fetal akinesia, limb contractures, hydramnios, and distended urinary bladder. Linkage to 5q and 9q34 loci has been excluded. Copyright 2002 Wiley-Liss, Inc.

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Year:  2003        PMID: 12548738     DOI: 10.1002/ajmg.a.10894

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  6 in total

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Journal:  J Autism Dev Disord       Date:  2017-09

2.  Dysregulation of the NRG1/ERBB pathway causes a developmental disorder with gastrointestinal dysmotility in humans.

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Journal:  J Clin Invest       Date:  2021-03-15       Impact factor: 14.808

3.  Lethal congenital contractural syndrome type 2 (LCCS2) is caused by a mutation in ERBB3 (Her3), a modulator of the phosphatidylinositol-3-kinase/Akt pathway.

Authors:  Ginat Narkis; Rivka Ofir; Esther Manor; Daniella Landau; Khalil Elbedour; Ohad S Birk
Journal:  Am J Hum Genet       Date:  2007-07-24       Impact factor: 11.025

4.  Lethal contractural syndrome type 3 (LCCS3) is caused by a mutation in PIP5K1C, which encodes PIPKI gamma of the phophatidylinsitol pathway.

Authors:  Ginat Narkis; Rivka Ofir; Daniella Landau; Esther Manor; Micha Volokita; Relly Hershkowitz; Khalil Elbedour; Ohad S Birk
Journal:  Am J Hum Genet       Date:  2007-07-24       Impact factor: 11.025

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Review 6.  Insight into the molecular genetics of myopia.

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  6 in total

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