RT Journal Article
T1 Headache as the presenting manifestation of Gorlin‐Goltz syndrome with diastematomyelia: A case report
A1 Ghosh, Ritwik
A1 León Ruiz, Moisés
A1 Purkait, Siktha
A1 Roy, Dipayan
A1 Ghosh, Tapas
A1 Benito León, Julián
AB Gorlin-Goltz syndrome (GGS) is an autosomal dominant multisystemic disease with high penetrance. Headache heralding GGS has been previously reported but without discussing potential sources. We report a patient with headache and a novel association (diastematomyelia), which helped with the diagnosis. A 46-year-old woman presented with persistent holocranial headache. On examination, countless hyperpigmented basal cell nevi over the face, pits over the palmar/plantar surface, and palmar and plantar keratosis were observed. A magnetic resonance imaging (MRI) of the spinal cord revealed diastematomyelia. Diagnosis of GGS was finally made. Headache and diastematomyelia should be included in the clinical picture of GGS.
PB Wiley
SN 2049-4173
SN 2049-4173
YR 2023
FD 2023-07-16
LK https://hdl.handle.net/20.500.14352/103315
UL https://hdl.handle.net/20.500.14352/103315
LA eng
NO Ghosh R, León-Ruiz M, Purkait S, Roy D, Ghosh T, Benito-León J. Headache as the presenting manifestation of Gorlin-Goltz syndrome with diastematomyelia: A case report. Neurol Clin Neurosci. 2023 Nov;11(6):328-331. doi: 10.1111/ncn3.12767. Epub 2023 Jul 16. PMID: 38130666
DS Docta Complutense
RD 20 ago 2024