Literature DB >> 17159510

Rhombencephalosynapsis presenting antenatally with ventriculomegaly/hydrocephalus in a likely case of Gomez-López-Hernández syndrome.

Sarah Bowdin1, Ethna Phelan, Rosemarie Watson, Kathryn M McCreery, William Reardon.   

Abstract

Rhombencephalosynapsis is a rare cerebellar malformation that can be associated with anomalies of the cerebral hemispheres and variable degrees of neurodevelopmental delay. A syndromic association, comprising rhombencephalosynapsis, developmental delay, scalp alopecia and trigeminal anaesthesia (Gomez-López-Hernández syndrome) has been described in seven individuals. We report the case of a 2-year-old boy with rhombencephalosynapsis, and review the evidence for a possible diagnosis of Gomez-López-Hernández syndrome. We also discuss other malformations reported in combination with rhombencephalosynapsis, and consider the possibility that a genetic aetiology for syndromic and nonsyndromic forms of rhombencephalosynapsis may be established with more detailed clinical and genetic studies.

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Year:  2007        PMID: 17159510     DOI: 10.1097/01.mcd.0000228426.97284.ff

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN: 0962-8827            Impact factor:   0.816


  1 in total

1.  Gómez-López-Hernández syndrome: reappraisal of the diagnostic criteria.

Authors:  Biayna Sukhudyan; Varsine Jaladyan; Gayane Melikyan; Jan Ulrich Schlump; Eugen Boltshauser; Andrea Poretti
Journal:  Eur J Pediatr       Date:  2010-07-23       Impact factor: 3.183

  1 in total

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