47 XYY and morning glory syndrome-A unique association

Journal of AAPOS

Volumn 13, Issue 4, 2009, Pages 406-407

  Chew, Fiona L M ^a   Visvaraja, Subrayan ^a  

^a UNIVERSITY MALAYA MEDICAL CENTRE   (Malaysia)

Author keywords

[No Author keywords available]

Indexed keywords

DESMOPRESSIN; LEVOTHYROXINE; THYROTROPIN; THYROXINE;

AGENESIS; APNEA; ARTICLE; BLOOD SAMPLING; CASE REPORT; CLINICAL FEATURE; CORPUS CALLOSUM; DIABETES INSIPIDUS; DISEASE ASSOCIATION; ENCEPHALOMENINGOCELE; EYE EXAMINATION; FACE DYSMORPHIA; FACE MALFORMATION; GESTATIONAL AGE; HOSPITAL ADMISSION; HOSPITAL DISCHARGE; HUMAN; HYPERTELORISM; HYPOTHYROIDISM; INFANT; KARYOTYPE 47,XYY; KARYOTYPING; MALE; MORNING GLORY SYNDROME; NUCLEAR MAGNETIC RESONANCE IMAGING; OPTIC DISK ANOMALY; PLASTIC SURGERY; PRIORITY JOURNAL; PUPIL REFLEX; SERUM OSMOLALITY; THYROTROPIN BLOOD LEVEL; THYROXINE BLOOD LEVEL; URINE OSMOLALITY; VOMITING;

ABNORMALITIES, MULTIPLE; ACROCALLOSAL SYNDROME; CHILD; ENCEPHALOCELE; EYE ABNORMALITIES; FRONTAL LOBE; HUMANS; HYPERTELORISM; KARYOTYPING; MAGNETIC RESONANCE IMAGING; MALE; MENINGOCELE; NOSE; OPTIC DISK; SYNDROME; XYY KARYOTYPE;

EID: 68349106935     PISSN: 10918531     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jaapos.2009.02.007     Document Type: Article

References (9)

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