Literature DB >> 31440883

Hypothalamic hamartomas and inner ear diverticula with X-linked stapes gusher syndrome - new associations?

Emily A Anderson1, Can Özütemiz2, Bradley S Miller3, Timothy J Moss3, David R Nascene2.   

Abstract

X-linked stapes gusher syndrome is a genetic form of deafness with distinct radiographic features on temporal bone CT. Hypothalamic hamartoma is a congenital glioneuronal anomaly of the hypothalamus. We report a potential association between these two rare anomalies that, to our knowledge, has not been reported. Two brothers presented with sensorineural hearing loss and almost identical inner ear and hypothalamic abnormalities, consistent with a diagnosis of X-linked stapes gusher syndrome and hypothalamic hamartoma. Genetic testing revealed identical mutations in the POU3F4 gene associated with X-linked stapes gusher syndrome. Furthermore, multiple vestibular diverticula were seen in both brothers, which have also not been reported with X-linked stapes gusher syndrome. This case suggests that POU3F4 mediated X-linked stapes gusher syndrome may also lead to multiple vestibular diverticula and hypothalamic hamartoma and, therefore, brain magnetic resonance imaging (MRI) could be considered in patients presenting with these inner ear findings.

Entities:  

Keywords:  Child; Computed tomography; Hamartoma; Hypothalamus; Magnetic resonance imaging; POU3F4; Sensorineural hearing loss; X-linked stapes gusher syndrome

Year:  2019        PMID: 31440883     DOI: 10.1007/s00247-019-04497-z

Source DB:  PubMed          Journal:  Pediatr Radiol        ISSN: 0301-0449


  8 in total

1.  Identification of a novel mutation in POU3F4 for prenatal diagnosis in a Chinese family with X-linked nonsyndromic hearing loss.

Authors:  Jianzhong Li; Jing Cheng; Yanping Lu; Yu Lu; Aiting Chen; Yi Sun; Dongyang Kang; Xin Zhang; Pu Dai; Dongyi Han; Huijun Yuan
Journal:  J Genet Genomics       Date:  2010-12       Impact factor: 4.275

2.  Development and survival of the endocrine hypothalamus and posterior pituitary gland requires the neuronal POU domain factor Brn-2.

Authors:  M D Schonemann; A K Ryan; R J McEvilly; S M O'Connell; C A Arias; K A Kalla; P Li; P E Sawchenko; M G Rosenfeld
Journal:  Genes Dev       Date:  1995-12-15       Impact factor: 11.361

3.  Brain 4: a novel mammalian POU domain transcription factor exhibiting restricted brain-specific expression.

Authors:  J M Mathis; D M Simmons; X He; L W Swanson; M G Rosenfeld
Journal:  EMBO J       Date:  1992-07       Impact factor: 11.598

4.  Somatic mutations in GLI3 and OFD1 involved in sonic hedgehog signaling cause hypothalamic hamartoma.

Authors:  Hirotomo Saitsu; Masaki Sonoda; Takefumi Higashijima; Hiroshi Shirozu; Hiroshi Masuda; Jun Tohyama; Mitsuhiro Kato; Mitsuko Nakashima; Yoshinori Tsurusaki; Takeshi Mizuguchi; Satoko Miyatake; Noriko Miyake; Shigeki Kameyama; Naomichi Matsumoto
Journal:  Ann Clin Transl Neurol       Date:  2016-03-24       Impact factor: 4.511

Review 5.  X-Linked Sensorineural Hearing Loss: A Literature Review.

Authors:  Virginia Corvino; Pasqualina Apisa; Rita Malesci; Carla Laria; Gennaro Auletta; Annamaria Franzé
Journal:  Curr Genomics       Date:  2018-08       Impact factor: 2.236

6.  Clinical and molecular characterization of POU3F4 mutations in multiple DFNX2 Chinese families.

Authors:  Yu Su; Xue Gao; Sha-Sha Huang; Jing-Ning Mao; Bang-Qing Huang; Jian-Dong Zhao; Dong-Yang Kang; Xin Zhang; Pu Dai
Journal:  BMC Med Genet       Date:  2018-09-04       Impact factor: 2.103

7.  Novel and De Novo Mutations Extend Association of POU3F4 with Distinct Clinical and Radiological Phenotype of Hearing Loss.

Authors:  Agnieszka Pollak; Urszula Lechowicz; Anna Kędra; Piotr Stawiński; Małgorzata Rydzanicz; Mariusz Furmanek; Małgorzata Brzozowska; Maciej Mrówka; Henryk Skarżyński; Piotr H Skarżyński; Monika Ołdak; Rafał Płoski
Journal:  PLoS One       Date:  2016-12-12       Impact factor: 3.240

8.  HDR syndrome with a novel mutation in GATA3 mimicking a congenital X-linked stapes gusher: a case report.

Authors:  Aram Yang; Jinsup Kim; Chang-Seok Ki; Sung Hwa Hong; Sung Yoon Cho; Dong-Kyu Jin
Journal:  BMC Med Genet       Date:  2017-10-26       Impact factor: 2.103

  8 in total
  3 in total

1.  A Case Series of X-Linked Deafness-2 with Sensorineural Hearing Loss, Stapes Fixation, and Perilymphatic Gusher: MR Imaging and Clinical Features of Hypothalamic Malformations.

Authors:  J-A Prat Matifoll; M Wilson; R Goetti; C Birman; B Bennett; E Peadon; A Prats-Uribe; K Prelog
Journal:  AJNR Am J Neuroradiol       Date:  2020-05-14       Impact factor: 3.825

Review 2.  New Imaging Findings of Incomplete Partition Type III Inner Ear Malformation and Literature Review.

Authors:  R Hong; Q Du; Y Pan
Journal:  AJNR Am J Neuroradiol       Date:  2020-05-28       Impact factor: 3.825

3.  Research progress of the transcription factor Brn4 (Review).

Authors:  Yuying Wu; Xunrui Zhang; Jue Wang; Guohua Jin; Xinhua Zhang
Journal:  Mol Med Rep       Date:  2021-01-05       Impact factor: 2.952

  3 in total

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