Literature DB >> 20685887

Duplication of the pituitary stalk in a patient with a heterozygous deletion of chromosome 14 harboring the thyroid transcription factor-1 gene.

S Accornero1, C Danesino, S Bastianello, I D'Errico, A Guala, L Chiovato.   

Abstract

Magnetic resonance imaging of the hypothalamic-pituitary region revealed a duplication of the pituitary stalk in a patient with a heterozygous deletion of chromosome 14 harboring the thyroid transcription factor-1 gene.

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Year:  2010        PMID： 20685887     DOI： 10.1210/jc.2010-0621

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN： 0021-972X            Impact factor:   5.958


  8 in total

1.  Pituitary duplication: a rare cause of precocious puberty.

Authors:  Leyla Akin; Mustafa Kendirci; Selim Doğanay; Selim Kurtoğlu; Bulent Tucer; Abdulhakim Coskun
Journal:  Childs Nerv Syst       Date:  2011-04-12       Impact factor: 1.475

2.  Persisting embryonal infundibular recess in a case of TITF-1 gene mutation.

Authors:  Elizabeth O'Mahony; Jonathan Ellenbogen; Shivaram Avula
Journal:  Neuroradiology       Date:  2022-02-24       Impact factor: 2.804

3.  Duplication of the Pituitary Gland: CT, MRI and DTI Findings and Updated Review of the Literature.

Authors:  Bettina L Serrallach; Ronald Rauch; Sarah K Lyons; Thierry A G M Huisman
Journal:  Brain Sci       Date:  2022-04-29

Review 4.  Benign Hereditary Chorea: An Update.

Authors:  Kathryn J Peall; Manju A Kurian
Journal:  Tremor Other Hyperkinet Mov (N Y)       Date:  2015-07-14

5.  Pituitary stalk interruption syndrome is characterized by genetic heterogeneity.

Authors:  Raja Brauner; Joelle Bignon-Topalovic; Anu Bashamboo; Ken McElreavey
Journal:  PLoS One       Date:  2020-12-03       Impact factor: 3.240

6.  Altered pituitary morphology as a sign of benign hereditary chorea caused by TITF1/NKX2.1 mutations.

Authors:  Steffi Thust; Liana Veneziano; Michael H Parkinson; Kailash P Bhatia; Elide Mantuano; Cristina Gonzalez-Robles; Indran Davagnanam; Paola Giunti
Journal:  Neurogenetics       Date:  2022-01-25       Impact factor: 2.660

Review 7.  A novel de novo mutation of the TITF1/NKX2-1 gene causing ataxia, benign hereditary chorea, hypothyroidism and a pituitary mass in a UK family and review of the literature.

Authors:  Liana Veneziano; Michael H Parkinson; Elide Mantuano; Marina Frontali; Kailash P Bhatia; Paola Giunti
Journal:  Cerebellum       Date:  2014-10       Impact factor: 3.847

8.  NKX2-1 New Mutation Associated With Myoclonus, Dystonia, and Pituitary Involvement.

Authors:  Péter Balicza; Zoltán Grosz; Viktor Molnár; Anett Illés; Dora Csabán; Andras Gézsi; Lívia Dézsi; Dénes Zádori; László Vécsei; Mária Judit Molnár
Journal:  Front Genet       Date:  2018-08-22       Impact factor: 4.599
  8 in total

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