Familial forms of thyroid dysgenesis among infants with congenital hypothyroidism [3]

New England Journal of Medicine

Volumn 343, Issue 6, 2000, Pages 441-442

  Castanet, Mireille ^a   Lyonnet, Stanislas ^b   Bonaïti Pellié, Catherine ^c   Polak, Michel ^a   Czernichow, Paul ^a   Léger, Juliane ^a  

^a HÔPITAL ROBERT DEBRÉ   (France)

^b HÔPITAL NECKER ENFANTS MALADES   (France)

^c INSTITUT GUSTAVE ROUSSY   (France)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL DOMINANT INHERITANCE; CONGENITAL HYPOTHYROIDISM; ECTOPIC THYROID GLAND; FAMILIAL DISEASE; HUMAN; LETTER; MEDICAL LITERATURE; PATHOGENESIS; PEDIGREE ANALYSIS; PRIORITY JOURNAL;

ABNORMALITIES; CHORISTOMA; CONGENITAL HYPOTHYROIDISM; FEMALE; FRANCE; HUMANS; HYPOTHYROIDISM; INFANT, NEWBORN; MALE; PEDIGREE; QUESTIONNAIRES; THYROID GLAND;

EID: 0034632713     PISSN: 00284793     EISSN: None     Source Type: Journal    
DOI: 10.1056/NEJM200008103430614     Document Type: Letter

References (5)

1. Familial athyreotic cretinism: Report of 3 cases
2. Hypothyroidism due to ectopy in siblings
3. The T/cbp null mouse: Thyroid-specific enhancer-binding protein is essential for the organogenesis of the thyroid, lung, ventral forebrain, and pituitary
4. Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia
5. PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis