Document Detail


Transient congenital hypothyroidism caused by biallelic mutations of the dual oxidase 2 gene in Japanese patients detected by a neonatal screening program.
MedLine Citation:
PMID:  18765513     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
CONTEXT: Mutations in dual oxidase (DUOX2) have been proposed as a cause of congenital hypothyroidism. Previous reports suggest that biallelic mutations of DUOX2 cause permanent congenital hypothyroidism and that monoallelic mutations cause transient congenital hypothyroidism. OBJECTIVE: To clarify the inheritance of hypothyroidism, we looked at the DUOX2 gene in patients with transient congenital hypothyroidism. DESIGN: DUOX2, thyroid peroxidase, Na+/I- symporter and dual oxidase maturation factor 2 genes were analyzed in eight patients with transient congenital hypothyroidism, using the PCR-amplified direct sequencing method. PATIENTS: The eight patients were found by a neonatal screening program. Six of these patients belonged to two independent families; the other two were unrelated. Their serum TSH values varied from 24.8-233.0 mU/liter. Six of the eight patients had a low serum freeT4 level (0.19-0.84 ng/dl). Seven of the eight patients were treated with thyroid hormone replacement therapy, which ceased to be necessary by 9 yr of age. RESULTS: Eight novel mutations were detected in the DUOX2 gene. Four patients in one family were compound heterozygous for p.L479SfsX2 and p.K628RfsX10. Two patients in a second family were compound heterozygous for p.K530X and p.[E876K;L1067S]. The two remaining unrelated patients were also compound heterozygous, for p.H678R/p.L1067S and p.A649E/p.R885Q, respectively. CONCLUSION: All eight patients had biallelic mutations in the DUOX2 gene. We find that loss of DUOX2 activity results in transient congenital hypothyroidism and that transient congenital hypothyroidism caused by DUOX2 mutations is inherited as an autosomal recessive trait.
Authors:
Yoshihiro Maruo; Hiroko Takahashi; Ikumi Soeda; Noriko Nishikura; Katsuyuki Matsui; Yoriko Ota; Yu Mimura; Asami Mori; Hiroshi Sato; Yoshihiro Takeuchi
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2008-09-02
Journal Detail:
Title:  The Journal of clinical endocrinology and metabolism     Volume:  93     ISSN:  0021-972X     ISO Abbreviation:  J. Clin. Endocrinol. Metab.     Publication Date:  2008 Nov 
Date Detail:
Created Date:  2008-11-06     Completed Date:  2008-12-31     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0375362     Medline TA:  J Clin Endocrinol Metab     Country:  United States    
Other Details:
Languages:  eng     Pagination:  4261-7     Citation Subset:  AIM; IM    
Affiliation:
Department of Pediatrics, Shiga University of Medical Science, Tsukinowa, Seta, Otsu, Shiga 520-2192, Japan. maruo@belle.shiga-med.ac.jp
Data Bank Information
Bank Name/Acc. No.:
GENBANK/AB379823;  AB379824;  AB379825;  AB379826;  AB379827;  AB379828;  AB379829;  AB379830
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MeSH Terms
Descriptor/Qualifier:
Child
Child, Preschool
Congenital Hypothyroidism / enzymology,  genetics*
Female
Genes, Recessive
Humans
Infant, Newborn
Iodide Peroxidase / genetics
Male
Molecular Sequence Data
Mutation*
NADPH Oxidase / genetics*
Neonatal Screening*
Polymerase Chain Reaction
Symporters / genetics
Thyrotropin / blood
Thyroxine / blood,  therapeutic use*
Triiodothyronine / blood
Chemical
Reg. No./Substance:
0/Symporters; 0/sodium-iodide symporter; 6893-02-3/Triiodothyronine; 7488-70-2/Thyroxine; 9002-71-5/Thyrotropin; EC 1.11.1.8/Iodide Peroxidase; EC 1.6.3.1/DUOX2 protein, human; EC 1.6.3.1/NADPH Oxidase

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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