Clinical, biochemical, and molecular findings in Argentinean patients with goitrous congenital hypothyroidism

Endocrine

Volumn 38, Issue 3, 2010, Pages 377-385

  Chiesa, Ana ^a   Rivolta, Carina M ^b   Targovnik, Héctor M ^b   Gruñeiro Papendieck, Laura ^a  

^a HOSPITAL DE NIÑOS RICARDO GUTIÉRREZ   (Argentina)

^b UNIVERSIDAD DE BUENOS AIRES   (Argentina)

Author keywords

Congenital goiter; DUOX2 gene; Hypothyroidism; Iodide organification defect; Mutation; Thyroglobulin gene; Thyroperoxidase gene

Indexed keywords

DUAL OXIDASE 2; DUAL OXIDASE A2; IODIDE; LIOTHYRONINE; OXIDOREDUCTASE; PERCHLORATE; THYROGLOBULIN; THYROID PEROXIDASE; THYROXINE; UNCLASSIFIED DRUG;

ARGENTINA; ARTICLE; CHILD; CLINICAL ASSESSMENT; CONGENITAL HYPOTHYROIDISM; CONTROLLED STUDY; DELAYED DIAGNOSIS; DISEASE SEVERITY; EARLY DIAGNOSIS; FOLLOW UP; GENE MUTATION; GENOTYPE PHENOTYPE CORRELATION; GOITER; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; MOLECULAR PATHOLOGY; MUTATIONAL ANALYSIS; NUCLEOTIDE SEQUENCE; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; THYROGLOBULIN BLOOD LEVEL; THYROID SCINTISCANNING;

EID: 79951670714     PISSN: 1355008X     EISSN: 15590100     Source Type: Journal    
DOI: 10.1007/s12020-010-9391-8     Document Type: Article

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