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Published in: Pediatric Radiology 1/2020

01-01-2020 | Magnetic Resonance Imaging | Case Report

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

Authors: Emily A. Anderson, Can Özütemiz, Bradley S. Miller, Timothy J. Moss, David R. Nascene

Published in: Pediatric Radiology | Issue 1/2020

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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.
Literature
1.
go back to reference Corvino V, Apisa P, Malesci R et al (2018) X-linked sensorineural hearing loss: a literature review. Curr Genomics 19:327–338CrossRef Corvino V, Apisa P, Malesci R et al (2018) X-linked sensorineural hearing loss: a literature review. Curr Genomics 19:327–338CrossRef
2.
go back to reference Saitsu H, Sonoda M, Higashijima T et al (2016) Somatic mutations in GLI3 and OFD1 involved in sonic hedgehog signaling cause hypothalamic hamartoma. Ann Clin Transl Neurol 3:356–365CrossRef Saitsu H, Sonoda M, Higashijima T et al (2016) Somatic mutations in GLI3 and OFD1 involved in sonic hedgehog signaling cause hypothalamic hamartoma. Ann Clin Transl Neurol 3:356–365CrossRef
3.
go back to reference Yang A, Kim J, Ki CS et al (2017) HDR syndrome with a novel mutation in GATA3 mimicking a congenital X-linked stapes gusher: a case report. BMC Med Genet 18:121CrossRef Yang A, Kim J, Ki CS et al (2017) HDR syndrome with a novel mutation in GATA3 mimicking a congenital X-linked stapes gusher: a case report. BMC Med Genet 18:121CrossRef
4.
go back to reference Su Y, Gao X, Huang SS et al (2018) Clinical and molecular characterization of POU3F4 mutations in multiple DFNX2 Chinese families. BMC Med Genet 19:157–167CrossRef Su Y, Gao X, Huang SS et al (2018) Clinical and molecular characterization of POU3F4 mutations in multiple DFNX2 Chinese families. BMC Med Genet 19:157–167CrossRef
5.
go back to reference Li J, Cheng J, Lu Y et al (2010) Identification of a novel mutation in POU3F4 for prenatal diagnosis in a Chinese family with X-linked nonsyndromic hearing loss. J Genet Genomics 37:787–793CrossRef Li J, Cheng J, Lu Y et al (2010) Identification of a novel mutation in POU3F4 for prenatal diagnosis in a Chinese family with X-linked nonsyndromic hearing loss. J Genet Genomics 37:787–793CrossRef
6.
go back to reference Pollak A, Lechowicz U, Kędra A et al (2016) Novel and de novo mutations extend association of POU3F4 with distinct clinical and radiological phenotype of hearing loss. PLoS One 11:e0166618CrossRef Pollak A, Lechowicz U, Kędra A et al (2016) Novel and de novo mutations extend association of POU3F4 with distinct clinical and radiological phenotype of hearing loss. PLoS One 11:e0166618CrossRef
7.
go back to reference Mathis JM, Simmons DM, He X et al (1992) Brain 4: a novel mammalian POU domain transcription factor exhibiting restricted brain-specific expression. EMBO J 11:2551–2561xCrossRef Mathis JM, Simmons DM, He X et al (1992) Brain 4: a novel mammalian POU domain transcription factor exhibiting restricted brain-specific expression. EMBO J 11:2551–2561xCrossRef
8.
go back to reference Schonemann MD, Ryan AK, McEvilly RJ et al (1995) Development and survival of the endocrine hypothalamus and posterior pituitary gland requires the neuronal POU domain factor Brn-2. Genes Dev 9:3122–3135CrossRef Schonemann MD, Ryan AK, McEvilly RJ et al (1995) Development and survival of the endocrine hypothalamus and posterior pituitary gland requires the neuronal POU domain factor Brn-2. Genes Dev 9:3122–3135CrossRef
Metadata
Title
Hypothalamic hamartomas and inner ear diverticula with X-linked stapes gusher syndrome - new associations?
Authors
Emily A. Anderson
Can Özütemiz
Bradley S. Miller
Timothy J. Moss
David R. Nascene
Publication date
01-01-2020
Publisher
Springer Berlin Heidelberg
Published in
Pediatric Radiology / Issue 1/2020
Print ISSN: 0301-0449
Electronic ISSN: 1432-1998
DOI
https://doi.org/10.1007/s00247-019-04497-z

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