Literature DB >> 830443

Universal permanent alopecia, psychomotor epilepsy, pyorrhea and mental subnormality.

M H Shokeir.   

Abstract

A syndrome of congenital and permanent universal alopecia, involving absence of scalp hair, eyebrows, eyelashes, axillary and pubic hair, and the rest of the body hair is reported. Mental subnormality was noted in eight and psychomotor epilepsy in seven out of 12 affected individuals. Pyorrhea was observed in all ascertained patients. No abnormality of nails or skin (apart from absence of hair) was noted. The disorder, which affected seven females and five males from six sibships, was transmitted through four generations. Utilizing the simple sib method, a ratio of 6/12 was obtained for affected individuals. The vertical transmission of the disorder, implication of both sexes, male to male transmission, and the 1:1 (affected: unaffected) segregation ratio support autosomal dominant inheritance. Penetrance appears to be complete.

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Year:  1977        PMID: 830443     DOI: 10.1111/j.1399-0004.1977.tb01271.x

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


  7 in total

1.  Acquired alopecia, mental retardation, short stature, microcephaly, and optic atrophy.

Authors:  R C Hennekam; E G Renckens-Wennen
Journal:  J Med Genet       Date:  1990-10       Impact factor: 6.318

2.  A familial syndrome of microcephaly, sparse hair, mental retardation, and seizures.

Authors:  A van Haeringen; J A Hurst; R Savidge; M Baraitser
Journal:  J Med Genet       Date:  1990-02       Impact factor: 6.318

3.  A new alopecia/mental retardation syndrome.

Authors:  M Baraitser; C O Carter; E M Brett
Journal:  J Med Genet       Date:  1983-02       Impact factor: 6.318

4.  Congenital universal alopecia, mental deficiency, and microcephaly in two sibs.

Authors:  R A Pfeiffer; J Völklein
Journal:  J Med Genet       Date:  1982-10       Impact factor: 6.318

5.  A novel locus for alopecia with mental retardation syndrome (APMR2) maps to chromosome 3q26.2-q26.31.

Authors:  A Wali; P John; A Gul; K Lee; M S Chishti; G Ali; M J Hassan; S M Leal; W Ahmad
Journal:  Clin Genet       Date:  2006-09       Impact factor: 4.438

6.  Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene and Review of Literature.

Authors:  Nesma M Elaraby; Hoda A Ahmed; Neveen A Ashaat; Sameh Tawfik; Mahmoud K H Ahmed; Nehal F Hassib; Engy A Ashaat
Journal:  J Mol Neurosci       Date:  2022-10-17       Impact factor: 2.866

7.  Mapping of a gene for alopecia with mental retardation syndrome (APMR3) on chromosome 18q11.2-q12.2.

Authors:  A Wali; G Ali; P John; K Lee; M S Chishti; S M Leal; W Ahmad
Journal:  Ann Hum Genet       Date:  2007-04-19       Impact factor: 1.670

  7 in total

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