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Results 1 - 8 of 8 for Central hypothyroidism
  1. TSHB gene 
    ... WG, Pohlenz J. Initially elevated TSH and congenital central hypothyroidism due to a homozygous mutation of the TSH ... RM, Polak M. New cases of isolated congenital central hypothyroidism due to homozygous thyrotropin beta gene mutations: a ...
    https://medlineplus.gov/genetics/gene/tshb - Genetics
  2. TPO gene 
    ... Citation on PubMed or Free article on PubMed Central Nascimento AC, Guedes DR, Santos CS, Knobel M, Rubio IG, Medeiros-Neto G. Thyroperoxidase gene mutations in congenital goitrous hypothyroidism with total and partial iodide organification defect. Thyroid. ...
    https://medlineplus.gov/genetics/gene/tpo - Genetics
  3. TSHR gene 
    ... Citation on PubMed or Free article on PubMed Central Bas VN, Cangul H, Agladioglu SY, Kendall M, Cetinkaya S, Maher ER, Aycan Z. Mild and severe congenital primary hypothyroidism in two patients by thyrotropin receptor (TSHR) gene ...
    https://medlineplus.gov/genetics/gene/tshr - Genetics
  4. PAX8 gene 
    ... Citation on PubMed or Free article on PubMed Central Ramos HE, ... of congenital hypothyroidism due to PAX8 gene loss-of-function mutations. ...
    https://medlineplus.gov/genetics/gene/pax8 - Genetics
  5. TG gene 
    ... Citation on PubMed or Free article on PubMed Central Caron P, Moya ... in fetal goitrous hypothyroidism. J Clin Endocrinol Metab. 2003 Aug;88(8): ...
    https://medlineplus.gov/genetics/gene/tg - Genetics
  6. NKX2-1 gene 
    ... van Landeghem F, DiLauro R, Gruters A. Choreoathetosis, hypothyroidism, and pulmonary alterations due to human NKX2-1 haploinsufficiency. J Clin Invest. 2002 Feb;109(4):475-80. doi: 10.1172/JCI14341. Citation on PubMed or Free article on PubMed Central Nettore IC, Mirra P, Ferrara AM, Sibilio A, ...
    https://medlineplus.gov/genetics/gene/nkx2-1 - Genetics
  7. SLC5A5 gene 
    ... Spitzweg C, Morris JC. Genetics and phenomics of hypothyroidism and goiter due ... Central Spitzweg C, Morris JC. The sodium iodide symporter: ...
    https://medlineplus.gov/genetics/gene/slc5a5 - Genetics
  8. SLC26A4 gene 
    ... these tissues. MedlinePlus Genetics provides information about Congenital hypothyroidism More About This Health Condition Dozens of SLC26A4 ... a loss of thyroid function from birth (congenital hypothyroidism). It is unclear whether Pendred syndrome, DFNB4, and ...
    https://medlineplus.gov/genetics/gene/slc26a4 - Genetics