Literature DB >> 35199208

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

Elizabeth O'Mahony1, Jonathan Ellenbogen2, Shivaram Avula3.   

Abstract

The thyroid transcription factor 1 (TITF-1) gene plays an important role in the development of the ventral forebrain, thyroid and lungs. Mutations of this gene are known to cause benign hereditary chorea (BHC) and can cause the full spectrum of abnormalities seen in the brain-thyroid-lung syndrome. Abnormalities of the ventral forebrain on imaging have been variably documented in the literature. Multiple previous reports describe a cystic pituitary mass, as well as duplication of the pituitary stalk and communication between an intrasellar cyst and the third ventricle. The initial MRI performed in our case was interpreted as an intrasellar cyst, but the high-resolution MRI performed later was able to resolve this as a persisting embryonal infundibular recess (PEIR), rather than the cystic pituitary mass which has previously been described. This case illustrates the role of the TITF-1 gene in the development of the pituitary and hypothalamus.
© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  Benign hereditary chorea; Hypothalamus; Persisting embryonal infundibular recess; TITF-1 gene mutation

Mesh:

Substances:

Year:  2022        PMID: 35199208     DOI: 10.1007/s00234-022-02905-0

Source DB:  PubMed          Journal:  Neuroradiology        ISSN: 0028-3940            Impact factor:   2.804


  8 in total

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

Authors:  S Accornero; C Danesino; S Bastianello; I D'Errico; A Guala; L Chiovato
Journal:  J Clin Endocrinol Metab       Date:  2010-08       Impact factor: 5.958

2.  Persisting Embryonal Infundibular Recess (PEIR): Two Case Reports and Systematic Literature Review.

Authors:  Francesco Belotti; Isabella Lupi; Mirco Cosottini; Claudia Ambrosi; Roberto Gasparotti; Fausto Bogazzi; Marco M Fontanella; Francesco Doglietto
Journal:  J Clin Endocrinol Metab       Date:  2018-07-01       Impact factor: 5.958

3.  Haploinsufficiency of NKX2-1 in Brain-Lung-Thyroid Syndrome with Additional Multiple Pituitary Dysfunction.

Authors:  Rathi Prasad; Adeline K Nicholas; Nadia Schoenmakers; John Barton
Journal:  Horm Res Paediatr       Date:  2019-11-08       Impact factor: 2.852

4.  Benign hereditary chorea: clinical and neuroimaging features in an Italian family.

Authors:  Elena Salvatore; Luigi Di Maio; Alessandro Filla; Alfonso M Ferrara; Carlo Rinaldi; Francesco Saccà; Silvio Peluso; Paolo E Macchia; Sabina Pappatà; Giuseppe De Michele
Journal:  Mov Disord       Date:  2010-07-30       Impact factor: 10.338

5.  Persisting embryonal infundibular recess.

Authors:  Andrej Steno; A John Popp; Stefan Wolfsberger; Vít'azoslav Belan; Juraj Steno
Journal:  J Neurosurg       Date:  2009-02       Impact factor: 5.115

Review 6.  Developmental Genes and Malformations in the Hypothalamus.

Authors:  Carmen Diaz; Luis Puelles
Journal:  Front Neuroanat       Date:  2020-11-26       Impact factor: 3.856

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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