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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

New Cases of Isolated Congenital Central Hypothyroidism Due to Homozygous Thyrotropin Beta Gene Mutations: A Pitfall to Neonatal Screening

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Author(s):
Ramos, Helton E. [1, 2] ; Labedan, Isabelle [3] ; Carre, Aurore [1] ; Castanet, Mireille [1] ; Guemas, Isabelle [4] ; Tron, Elodie [1] ; Madhi, Fouad [3] ; Delacourt, Christophe [5] ; Maciel, Rui M. B. [2] ; Polak, Michel [1, 6]
Total Authors: 10
Affiliation:
[1] Univ Paris 05, Pediat Endocrine Unit, Paris - France
[2] Univ Fed Sao Paulo, Dept Med, Div Endocrinol, Mol Endocrinol Lab, Sao Paulo - Brazil
[3] Ctr Hosp Creteil, Serv Pediat, Creteil - France
[4] CH Lens, Serv Pediat, Lens - France
[5] Hop Necker Enfants Malad, Serv Pneumol Pediat, F-75743 Paris 15 - France
[6] Hop Necker Enfants Malad, AP HP, Ctr Malad Endocriniennes Rares Croissance, Pediat Endocrine Unit, INSERM, U845, F-75743 Paris - France
Total Affiliations: 6
Document type: Journal article
Source: THYROID; v. 20, n. 6, p. 639-645, JUN 2010.
Web of Science Citations: 10
Abstract

Background: Congenital central hypothyroidism (CCH) is a rare condition that is often diagnosed in late childhood in countries where neonatal screening programs rely solely on detecting thyrotropin (TSH) elevation. TSH beta gene mutation is one of the causes of CCH. We describe two cases of c.Q49X mutation and three cases of c.C105Vfs114X mutation in exon 3 of the TSH beta-subunit gene. Summary: We found two different TSH beta gene mutations in two families. In one family, we identified a missense mutation in exon 3 leading to a premature stop at position 49 (c.Q49X) in the two affected twins. In the other family, the three affected siblings had a 313delT nucleotide deletion leading to a frame shift responsible for premature termination at codon 114 (c.C105Vfs114X); neonatal screening showed very low TSH levels in all three patients. The presence of inappropriately low TSH levels at birth in the three affected members of the second family raises questions about the value of the TSH level for CCH screening. Conclusions: The marked phenotypic variability in patients with the c.Q49X mutation suggests modulation by interacting genes and/or differences in the genetic background. TSH beta gene mutations should be suspected in neonates with inappropriately low TSH levels. (AU)