Hypergonadotropic hypogonadism in a boy with Fanconi anemia with growth hormone deficiency and pituitary stalk interruption [1]

Journal of Pediatrics

Volumn 140, Issue 2, 2002, Pages 277-

  Massa, Guy G ^a   Heinrichs, C ^a   Fabiola, Reine ^a   Vamos, E ^a   Van Vliet, G ^a  

^a HOP UNIV DES ENFANTS REINE FABIOLA   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

GROWTH HORMONE; LEVOTHYROXINE;

CASE REPORT; CHILD; CLINICAL FEATURE; DISEASE ASSOCIATION; FANCONI ANEMIA; GERM CELL; GROWTH HORMONE DEFICIENCY; HUMAN; HYPERGONADOTROPIC HYPOGONADISM; HYPOGONADISM; INFUNDIBULUM; LETTER; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; PUBERTY;

EID: 0036189668     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1067/mpd.2002.119174     Document Type: Letter

References (5)

1. Growth hormone deficiency caused by pituitary stalk interruption in Fanconi's anemia
2. Gonadal function in two siblings with Fanconi's anemia
3. Growth hormone deficiency in one of two siblings with Fanconi's anaemia complementation group FA-D
4. Studies of malformation syndrome of man XLVII: Disappearance of spermatogonia in the Fanconi anemia syndrome
5. Fanconi anemia complementation group C is required for proliferation of murine primordial germ cells