American Journal of Medical Genetics · 2002 · 13 citations · 12 references
MedicineOphthalmologyPathologyOcular DiseaseOcular PathologyOphthalmic PathologyCerebrovascular DiseaseMelanocytic LesionsNeurocutaneous SyndromesPigmentary DisordersVascular AnomaliesVascular MalformationsBlaschko LinesCavernous Carotid AneurysmCavernous Sinus InvolvementCavernous Sinus TumorsIncontinentia PigmentiNevoid Skin DisordersOphthalmic ManifestationsSkin Hyperextensibility
A 24-year-old woman presented with bilateral giant intracavernous carotid artery aneurysms manifesting as a cavernous sinus syndrome on the left side, and anisocoria, ophthalmic pain, and oculomotor paresis on the left side. Physical examination showed mild hyperextensibility of the metacarpophalangeal joints, amelogenesis imperfecta, and hyperpigmentation following Blaschko lines. Analysis of the NEMO gene for incontinentia pigmenti syndrome and of collagen III for Ehlers-Danlos type IV was normal. Skewed X-inactivation patterns in blood lymphocytes were detected. To the best of our knowledge, this association of linear hyperpigmentation and cerebral aneurysms has never been previously reported.
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Genomic rearrangement in NEMO impairs NF-κB activation and is a cause of incontinentia pigmenti
Asma Smahi, Nina S. Heiss, Petra Kioschis et al. · Nature · 2000 · 743 citations
Jonathan Zonana, Melissa E. Elder, Lynda C. Schneider et al. · The American Journal of Human Genetics · 2000 · 523 citations · Full text
Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism.
I. T. Thomas, Jaime L. Frías, E S Cantú et al. · PubMed · 1989 · 157 citations
Eli Hatchwell, D Robinson, John A. Crolla et al. · Journal of Medical Genetics · 1996 · 116 citations · Full text