Duplication of the Pituitary Stalk in a Patient with a Heterozygous Deletion of Chromosome 14 Harboring the Thyroid Transcription Factor-1 Gene

Author:

Accornero S.1,Danesino C.2,Bastianello S.3,D'Errico I.3,Guala A.4,Chiovato L.1

Affiliation:

1. Unit of Internal Medicine and Endocrinology (S.A., L.C.), Fondazione Salvatore Maugeri Instituto di Ricovero e Cura a Carattere Scientifico (IRCCS), University of Pavia, 27100 Pavia, Italy;

2. Medical Genetics (C.D.), IRCCS Fondazione Policlinico S. Matteo and University of Pavia, 27100 Pavia, Italy;

3. Unit of Neuroradiology (S.B., I.D.), Fondazione Casimiro Mondino IRCCS, University of Pavia, 27100 Pavia, Italy;

4. Struttura Operativa Complessa Pediatria (A.G.), Ospedale Castelli, 28921 Verbania, Italy

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference4 articles.

1. Mutations in TITF-1 are associated with benign hereditary chorea.;Breedveld;Hum Mol Genet,2002

2. Deletion of PAX9 and oligodontia: a third family and review of the literature.;Guala;Int J Paediatr Dent,2008

3. TTF-1 regulates growth hormone and prolactin transcription in the anterior pituitary gland.;Lee;Biochem Biophys Res Commun,2007

4. Genetic regulation of pituitary gland development in human and mouse.;Kelberman;Endocr Rev,2009

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