Less known aspects of central hypothyroidism: Part 2 - Congenital etiologies.

Benvenga, Salvatore; Klose, Marianne; Vita, Roberto; Feldt-Rasmussen, Ulla

Benvenga, Salvatore; Klose, Marianne; Vita, Roberto; Feldt-Rasmussen, Ulla.

Affiliation

Benvenga S; Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
Klose M; Master Program on Childhood, Adolescent and Women's Endocrine Health, University of Messina, Messina, Italy.
Vita R; Interdepartmental Program of Molecular & Clinical Endocrinology, and Women's Endocrine Health, University Hospital Policlinico G. Martino, Messina, Italy.
Feldt-Rasmussen U; Department of Medical Endocrinology and Metabolism, Rigshospitalet, National University Hospital, Copenhagen University, Copenhagen, Denmark.

J Clin Transl Endocrinol ; 14: 5-11, 2018 Dec.

Article in En | MEDLINE | ID: mdl-30294553

Key words

ACTH, adrenocorticotropin hormone; ALGS, arteriohepatic dysplasia; CH, central hypothyroidism; Central hypothyroidism; Congenital hypothyroidism; DWS, Dandy-Walker syndrome; FT3, free triiodothyronine; FT4, free thyroxine; GH, growth hormone; HCG, human chorionic gonadotropin; Hypopituitarism; IGDF1, immunogobulin superfamily member 1; PC1/3, proprotein convertase 1/3; PWS, Prader-Willi syndrome; ROHHAD, rapid-onset obesity with hypoventilation, hypothalamic dysfunction and autonomic dysregulation; SCD, sickle cell anemia; SMMCIS, solitary median maxillary central incisor syndrome; SOD, septo-optic dysplasia; SWS, Sturge-Weber syndrome; TRH, TSH-releasing hormone; TSH, thyrotropin; TT3, total triiodothyronine; TT4, total thyroxine; Thyrotropin deficiency

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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Etiology_studies Language: En Journal: J Clin Transl Endocrinol Year: 2018 Document type: Article Affiliation country: Italy Country of publication: Netherlands

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