Literature DB >> 18361769

More than skin deep: a case of congenital lamellar ichthyosis, lymphatic malformation, and other abnormalities.

Katherine Small1, Howard Ginsburg, M Alba Greco, Carmen Sarita-Reyes, Gabriel Kupchik, Francine Blei.   

Abstract

Consanguinity allows for the expression of rare genetic disorders. We present the first case of an infant, born to consanguineous parents, with congenital lamellar ichthyosis, congenital lymphatic malformation, congenital hypothyroidism, bilateral megaureter, benign external hydrocephalus, and syrinx of the spinal cord. We review the disorders, examine their genetic causes, and explore the genetic connection among them.

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Year:  2008        PMID: 18361769     DOI: 10.1089/lrb.2007.1020

Source DB:  PubMed          Journal:  Lymphat Res Biol        ISSN: 1539-6851            Impact factor:   2.589


  2 in total

1.  Exome Analysis Identifies a Novel Compound Heterozygous Alteration in TGM1 Gene Leading to Lamellar Ichthyosis in a Child From Saudi Arabia: Case Presentation.

Authors:  Sami Raja Alallasi; Amal A Kokandi; Babajan Banagnapali; Noor Ahmad Shaik; Bandar Ali Al-Shehri; Nuha Mohammad Alrayes; Jumana Yousuf Al-Aama; Musharraf Jelani
Journal:  Front Pediatr       Date:  2019-02-21       Impact factor: 3.418

2.  Congenital lamellar ichthyosis in Tunisia is caused by a founder nonsense mutation in the TGM1 gene.

Authors:  Nacim Louhichi; Ikhlass Hadjsalem; Slaheddine Marrakchi; Fatma Trabelsi; Abderrahmen Masmoudi; Hamida Turki; Faiza Fakhfakh
Journal:  Mol Biol Rep       Date:  2012-11-29       Impact factor: 2.316

  2 in total

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