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.

Afiliación

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 en En | MEDLINE | ID: mdl-30294553

Palabras clave

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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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Etiology_studies Idioma: En Revista: J Clin Transl Endocrinol Año: 2018 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Países Bajos

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