Progressive extrapyramidal disorder with primary hypogonadism and alopecia in sibs: A new syndrome?

American Journal of Medical Genetics

Volumn 62, Issue 1, 1996, Pages 54-57

  Devriendt, Koenraad ^a   Legius, Eric ^a   Fryns, Jean Pierre ^a,b  

^a UNIVERSITY OF LEUVEN   (Belgium)

^b CENTER FOR HUMAN GENETICS   (Belgium)

Author keywords

alopecia; autosomal recessive inheritance; hypogonadism; neurological symptoms

Indexed keywords

17 OXOSTEROID; CHORIONIC GONADOTROPIN; ESTRADIOL; FOLLITROPIN; GONADOTROPIN; METHYLTESTOSTERONE; SEX HORMONE;

ADULT; ALOPECIA; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; CONSANGUINEOUS MARRIAGE; DEMENTIA; EXTRAPYRAMIDAL SYNDROME; FEMALE; HUMAN; HYPOGONADISM; MALE; MICROCEPHALY; MOTOR DYSFUNCTION; PRIORITY JOURNAL; SEX HORMONE DETERMINATION; SIBLING; SYNDROME;

ADULT; ALOPECIA; BASAL GANGLIA DISEASES; CONSANGUINITY; DISEASE PROGRESSION; FEMALE; FOLLOW-UP STUDIES; HUMANS; HYPOGONADISM; MALE; MIDDLE AGED; SYNDROME;

EID: 0029866260     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19960301)62:1<54::AID-AJMG11>3.0.CO;2-U     Document Type: Article

References (7)

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