Literature DB >> 5173317

The characterization of hereditary abnormalities of keratin: Clouston's ectodermal dysplasia.

J M Reynold, M B Gold, C R Scriver.   

Abstract

Ectodermal dysplasia of the Clouston type is a disease caused by a single dose of an autosomal dominant gene. It appears to involve only the skin and its appendages. An investigation of the physical and chemical abnormalities of the hair protein in this disease is beginning to throw some light on the action of the gene involved.

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Year:  1971        PMID: 5173317

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN: 0547-6844


  5 in total

1.  Letters:Structural hair abnormalities in hidrotic ectodermal dysplasia (HED).

Authors:  L Wilsch; E Haneke; G Schaidt
Journal:  Arch Dermatol Res       Date:  1977-07-21       Impact factor: 3.017

2.  Loss of a homologous group of proteins in a dominantly inherited ectodermal malformation.

Authors:  H S Tenenhouse; R J Gold
Journal:  Biochem J       Date:  1976-10-01       Impact factor: 3.857

3.  [Morphological and biochemical investigations of hairs in inborn errors of amino acid metabolism (author's transl)].

Authors:  L G Wiest; P Lutz; E G Jung; N Paweletz
Journal:  Arch Dermatol Res       Date:  1976-07-26       Impact factor: 3.017

4.  Ectodermal dysplasia - Maxillary and mandibular alveolar reconstruction with dental rehabilitation: A case report and review of the literature.

Authors:  Sanjeev N Deshpande; Vikas Kumar
Journal:  Indian J Plast Surg       Date:  2010-01

5.  A Clinico-Epidemiological Study of Scalp Hair Loss in Children (0-18 Years) in Kota Region, South-East Rajasthan.

Authors:  Manoj Kumar Sharma; Savera Gupta; Ramesh Kumar; Anil Kumar Singhal; Suresh Kumar Jain; Mukul Sharma
Journal:  Indian J Dermatol       Date:  2019 Jul-Aug       Impact factor: 1.494

  5 in total

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