Publication:
Gomez-Lopez-Hernandez Syndrome: A Rare Cause of Bilateral Nonscarring Alopecia

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dc.contributor.authorEKİNCİ, GAZANFER
dc.contributor.authorÜNVER, OLCAY
dc.contributor.authorERGUN, SAFİYE ATLAS TÜLİN
dc.contributor.authorsSaricam, Merve Hatun; Tekin, Burak; Unver, Olcay; Ekinci, Gazanfer; Ergun, Tulin
dc.date.accessioned2022-03-13T12:47:20Z
dc.date.accessioned2026-01-11T13:43:04Z
dc.date.available2022-03-13T12:47:20Z
dc.date.issued2015
dc.description.abstractGomez-Lopez-Hernandez syndrome is a rare neurocutaneous disorder characterized by the triad of rhombencephalosynapsis, parietal alopecia, and trigeminal anesthesia. We report a 16-year-old girl with bilateral parietotemporal alopecia in whom cranial magnetic resonance imaging revealed rhombencephalosynapsis, suggesting a diagnosis of Gomez-Lopez-Hernandez syndrome. Neurologic examination and neuroimaging may be warranted in select patients with parietal alopecia to exclude this uncommon entity.
dc.identifier.doi10.1111/pde.12678
dc.identifier.eissn1525-1470
dc.identifier.issn0736-8046
dc.identifier.pubmed26391554
dc.identifier.urihttps://hdl.handle.net/11424/238060
dc.identifier.wosWOS:000365526000007
dc.language.isoeng
dc.publisherWILEY
dc.relation.ispartofPEDIATRIC DERMATOLOGY
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.titleGomez-Lopez-Hernandez Syndrome: A Rare Cause of Bilateral Nonscarring Alopecia
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPagee254
oaire.citation.issue6
oaire.citation.startPagee251
oaire.citation.titlePEDIATRIC DERMATOLOGY
oaire.citation.volume32

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