Literature DB >> 14476762

Familial congenital alopecia, epilepsy, mental retardation with unusual electroencephalograms.

E J MOYNAHAN.   

Abstract

Entities:  

Keywords:  ALOPECIA/in infancy and childhood; EPILEPSY/in infancy and childhood

Mesh:

Year:  1962        PMID: 14476762      PMCID: PMC1896622     

Source DB:  PubMed          Journal:  Proc R Soc Med        ISSN: 0035-9157


× No keyword cloud information.
  5 in total

1.  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

2.  Congenital alopecia, psychomotor retardation, convulsions in two sibs of a consanguineous marriage.

Authors:  T Perniola; G Krajewska; F Carnevale; M Lospalluti
Journal:  J Inherit Metab Dis       Date:  1980       Impact factor: 4.982

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.  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

5.  Congenital atrichia associated with nevus flammeus: A rare association.

Authors:  Ep Raj Kirit; Anchala Parthasaradhi
Journal:  Indian Dermatol Online J       Date:  2014-10
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.