A 46,XX fetus with external female and internal male genitalia, facial dysmorphic features and mildly dilated lateral ventricles of the brain: A new syndrome?

Clinical Dysmorphology

Volumn 10, Issue 3, 2001, Pages 215-217

  Becker, K ^a,c   Seller, M J ^b,d   Pal, K ^a   Davies, A F ^a  

^a GUY'S AND ST THOMAS' NHS FOUNDATION TRUST   (United Kingdom)

^b KING'S COLLEGE LONDON   (United Kingdom)

^c NORTHWICK PARK HOSPITAL   (United Kingdom)

^d GUY S HOSPITAL   (United Kingdom)

Author keywords

Male sexual development; Sex reversal; XX males

Indexed keywords

ARTICLE; BRAIN VENTRICLE DILATATION; CASE REPORT; CLINICAL FEATURE; FACE DYSMORPHIA; FETUS; HUMAN; MALE GENITAL SYSTEM; PRIORITY JOURNAL; SEX TRANSFORMATION; SYNDROME; XX MALE;

EID: 0034951301     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-200107000-00012     Document Type: Article

References (4)

1. Molecular, cytogenetic, and clinical characterisation of six XX males including one prenatal diagnosis
2. A regulatory cascade hypothesis for mammalian sex determination: SRY represses a negative regulator of male development
3. Sex determination in humans
4. An autosomal or X linked mutation results in true hermaphrodites and 46,XX males in the same family