dc.creatorSilva, J. Enrique
dc.creatorSantelices, Raül
dc.creatorKishihara, Michizo
dc.creatorSchneider, Arthur
dc.date.accessioned2019-01-29T14:47:05Z
dc.date.available2019-01-29T14:47:05Z
dc.date.created2019-01-29T14:47:05Z
dc.date.issued1984
dc.identifierJournal of Clinical Endocrinology and Metabolism, Volumen 58, Issue 3, 2018, Pages 526-534
dc.identifier19457197
dc.identifier0021972X
dc.identifier10.1210/jcem-58-3-526
dc.identifierhttps://repositorio.uchile.cl/handle/2250/160536
dc.description.abstractWe characterized the abnormal thyroglobulin (TG) in the thyroid and serum of a 12-yr-old girl with a large sporadic multinodular goiter first noted at age 4 yr. She developed normallyand had no clinical evidence of hypothyroidism. However, her serum T4 was less than 1.0/µg/dl, T3 was 125 ng/ dl, and TSH was 155 µU/ml. Serum PBI was 9.7 /µg/dl, and more than 90% was not extractable with butanol. The 24-h radioactive iodine uptake was 55%, not dischargeable by perchlorate. Hormone formation was tested by the administration of 131I before surgery. [131I]T4 and [131I]T3) but not 131I-labeled iodotyrosines, were present in the thyroidal venous blood. Hydrolysis of 10,000 × g supernatants from three randomly obtained samples of the goiter revealed 66–77% of the 131I asiodotyrosines, 2–4% as iodothyronines, and 10–12% as undigestable material; the MIT to DIT ratio ranged from 3.1–8.7, and the T4 to T3 ratio rangedfrom 2.3–8.3. The TG level was 2.5 mg/g in the goiter and 9.4 /µg/ml in the seru
dc.languageen
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceJournal of Clinical Endocrinology and Metabolism
dc.subjectEndocrinology, Diabetes and Metabolism
dc.subjectBiochemistry
dc.subjectEndocrinology
dc.subjectClinical Biochemistry
dc.subjectBiochemistry (medical)
dc.titleLow molecular weight thyroglobulin leading to a goiter in a 12-year-old girl
dc.typeArtículo de revista


Este ítem pertenece a la siguiente institución