Primary hypothyroidism and nipple hypoplasia in a girl with Wolcott-Rallison syndrome

European Journal of Pediatrics

Volumn 173, Issue 4, 2014, Pages 529-531

  Špehar Uroić, Anita ^a   Mulliqi Kotori, Vjosa ^b   Rojnić Putarek, Nataša ^c   Kušec, Vesna ^c   Dumić, Miroslav ^c  

^a KBC Zagreb   (Croatia)

^b UNIVERSITY CLINICAL CENTER OF KOSOVO   (Serbia)

^c UNIVERSITY OF ZAGREB   (Croatia)

Author keywords

EIF2AK3; Nipple hypoplasia; Primary hypothyroidism; Wolcott Rallison syndrome

Indexed keywords

INSULIN; EIF2AK3 PROTEIN, HUMAN; PROTEIN KINASE R;

ANEMIA; ARTICLE; BREAST; CASE REPORT; CHILD; DIABETES MELLITUS; EIF2AK3 GENE; EXON; FEMALE; FULMINANT HEPATIC FAILURE; GENE; GENE MUTATION; GENETIC ANALYSIS; HUMAN; HYPOPLASIA; HYPOTHYROIDISM; INSULIN TREATMENT; KIDNEY DISEASE; LIVER DYSFUNCTION; LIVER FAILURE; MALE; MICROCEPHALY; NEWBORN; NIPPLE; PANCREAS EXOCRINE INSUFFICIENCY; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SHORT STATURE; SKELETON MALFORMATION; SPEECH DEVELOPMENT; THYROID DYSGENESIS; WOLCOTT RALLISON SYNDROME; CHONDRODYSPLASIA; CONSANGUINITY; EPIPHYSIS; GENETICS; INSULIN DEPENDENT DIABETES MELLITUS; MUTATION;

CHILD; CHILD, PRESCHOOL; CONSANGUINITY; DIABETES MELLITUS, TYPE 1; EIF-2 KINASE; EPIPHYSES; FEMALE; HUMANS; HYPOTHYROIDISM; MALE; MUTATION; NIPPLES; OSTEOCHONDRODYSPLASIAS; THYROID DYSGENESIS;

EID: 84897026166     PISSN: 03406199     EISSN: 14321076     Source Type: Journal    
DOI: 10.1007/s00431-013-2189-y     Document Type: Article

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