Clinical description of infants with congenital hypothyroidism and iodide organification defects

Hormone Research

Volumn 70, Issue 4, 2008, Pages 240-248

  Cavarzere, Paolo ^a,b   Castanet, Mireille ^a   Polak, Michel ^a   Raux Demay, Marie Charles ^c   Cabrol, Sylvie ^c   Carel, Jean Claude ^d   Léger, Juliane ^d   Czernichow, Paul ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

^b UNIVERSITY OF VERONA   (Italy)

^c ASSISTANCE PUBLIQUE HÔPITAUX DE PARIS   (France)

^d HÔPITAL ROBERT DEBRÉ   (France)

Author keywords

Congenital hypothyroidism; Dyshormonogenesis; Goiter; Iodide organification defect; Perchlorate discharge test

Indexed keywords

IODIDE; LEVOTHYROXINE; PERCHLORATE;

ABDOMINAL DISTENSION; ARTICLE; CLINICAL FEATURE; COMPARATIVE STUDY; CONGENITAL HYPOTHYROIDISM; CONSTIPATION; CONTROL GROUP; CONTROLLED STUDY; DISEASE SEVERITY; DRUG WITHDRAWAL; ENZYME ACTIVITY; FEEDING BEHAVIOR; FEMALE; FRANCE; GENOTYPE PHENOTYPE CORRELATION; GOITER; HEARING IMPAIRMENT; HOARSENESS; HUMAN; INCIDENCE; INFANT; IODIDE ORGANIFICATION DEFECT; JAUNDICE; LANGUAGE DISABILITY; MAJOR CLINICAL STUDY; MALE; MUSCLE HYPOTONIA; PRIORITY JOURNAL; SCINTIGRAPHY; THYROID DISEASE; UMBILICAL HERNIA; UNDERWEIGHT;

CONGENITAL HYPOTHYROIDISM; FEMALE; HUMANS; INFANT; INFANT, NEWBORN; IODIDES; MALE; PARIS; RETROSPECTIVE STUDIES; THYROID GLAND;

EID: 50849110142     PISSN: 03010163     EISSN: None     Source Type: Journal    
DOI: 10.1159/000151597     Document Type: Article

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