Iodide transport defect (ITD) is a rare disorder characterised by an inability of the thyroid to maintain an iodide gradient across the basolateral membrane of thyroid follicular cells, that often results in congenital hypothyroidism. When present the defect is also found in the salivary glands and gastric mucosa and it has been shown to arise from abnormalities of the sodium/iodide symporter (NIS).

Tonacchera, M., Agretti, P., de Marco, G., Elisei, R., Perri, A., Ambrogini, E., et al. (2003). Congenital hypothyroidism due to a new deletion in the sodium/iodide symporter protein. CLINICAL ENDOCRINOLOGY, 59(4), 500-506.

Congenital hypothyroidism due to a new deletion in the sodium/iodide symporter protein

MANCA BITTI, MARIA LUISA;
2003-10-01

Abstract

Iodide transport defect (ITD) is a rare disorder characterised by an inability of the thyroid to maintain an iodide gradient across the basolateral membrane of thyroid follicular cells, that often results in congenital hypothyroidism. When present the defect is also found in the salivary glands and gastric mucosa and it has been shown to arise from abnormalities of the sodium/iodide symporter (NIS).
ott-2003
Pubblicato
Rilevanza internazionale
Articolo
Esperti non anonimi
Settore MED/38 - PEDIATRIA GENERALE E SPECIALISTICA
English
Con Impact Factor ISI
Iodides; Animals; COS Cells; Exons; Humans; Thyroid Gland; Gene Deletion; Symporters; Transfection; Congenital Hypothyroidism; Heterozygote; Adult; Cercopithecus aethiops; Introns; Family; Hypothyroidism; Immunohistochemistry; Female
Tonacchera, M., Agretti, P., de Marco, G., Elisei, R., Perri, A., Ambrogini, E., et al. (2003). Congenital hypothyroidism due to a new deletion in the sodium/iodide symporter protein. CLINICAL ENDOCRINOLOGY, 59(4), 500-506.
Tonacchera, M; Agretti, P; de Marco, G; Elisei, R; Perri, A; Ambrogini, E; De Servi, M; Ceccarelli, C; Viacava, P; Refetoff, S; Panunzi, C; MANCA BITTI, Ml; Vitti, P; Chiovato, L; Pinchera, A
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/103000
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