Intrauterine therapy of goitrous hypothyroidism in a boy with a new compound heterozygous mutation (Y453D and C800R) in the thyroid peroxidase gene. A long-term follow-up

American Journal of Obstetrics and Gynecology

Volumn 193, Issue 3, 2005, Pages 857-858

  Börgel, Kirsten ^a   Pohlenz, Joachim ^b   Holzgreve, Wolfgang ^c   Bramswig, Jurgen H ^a  

^a UNIVERSITY HOSPITAL MÜNSTER   (Germany)

^b UNIVERSITY MEDICAL CENTER MAINZ   (Germany)

^c UNIVERSITY OF BASEL   (Switzerland)

Author keywords

Congenital hypothyroidism; Fetal goiter; Intrauterine therapy; TPO gene

Indexed keywords

LEVOTHYROXINE; THYROID PEROXIDASE;

ADULT; ARTICLE; CASE REPORT; FEMALE; FETUS (ANATOMY); FOLLOW UP; GENE MUTATION; GESTATIONAL AGE; HUMAN; HYDRAMNIOS; HYPOTHYROIDISM; PRIORITY JOURNAL; VAGINAL DELIVERY; WHIPLASH INJURY;

ADULT; CONGENITAL HYPOTHYROIDISM; FEMALE; FETAL DISEASES; FETAL THERAPIES; FOLLOW-UP STUDIES; GOITER; HUMANS; HYPOTHYROIDISM; INJECTIONS; IODIDE PEROXIDASE; MALE; POLYHYDRAMNIOS; PREGNANCY; RETREATMENT; THYROXINE;

EID: 24344460352     PISSN: 00029378     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ajog.2005.01.060     Document Type: Article

References (3)

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2. P. Caron, C.M. Moya, D. Malet, V.J. Gutnisky, B. Chabardes, and C.M. Rivolta Compound heterozygous mutations in the thyroglobulin gene (1143delC and 6725G->A [R2223H]) resulting in fetal goitrous hypothyroidism J Clin Endocrinol Metab 88 2003 3546 3553
3. C. Gruner, A. Kollert, L. Wildt, H.G. Dorr, E. Beinder, and N. Lang Intrauterine treatment of fetal goitrous hypothyroidism controlled by determination of thyroid-stimulating hormone in fetal serum. A case report and review of the literature Fetal Diagn Ther 16 2001 47 51