Incontinentia Pigmenti and Norrie Disease: Pathogenesis, Diagnosis, and Treatment

نویسندگان

چکیده

Incontinentia pigmenti is a very rare X-linked dominant inherited disease characterized by skin lesions, retinal pathologies, central nervous system anomalies, and dental problems. Norrie recessive severe vitreoretinal dysplasia in both eyes at birth. In diseases, patients can apply to the clinic with nystagmus, leukocoria, microphthalmia, detachment an early age. this review, disease, which are pediatric vascular investigated detail.

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Concurrence of Incontinentia Pigmenti and Behçet's Disease.

We report here a rare case of incontinentia pigmenti (IP) in a 10-year-old girl who developed Behçet's disease. IP was diagnosed in infancy and Behçet's disease was diagnosed at 10 years of age. The initial presentations of Behçet's disease were spiking fever and recurrent painful oral and genital ulcers that were refractory to antibiotics. After corticosteroid treatment, her fever subsided and...

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Incontinentia pigmenti*

Incontinentia pigmenti is a rare genodermatosis in which the skin involvement occurs in all patients. Additionally, other ectodermal tissues may be affected, such as the central nervous system, eyes, hair, nails and teeth. The disease has a X-linked dominant inheritance pattern and is usually lethal to male fetuses. The dermatological findings occur in four successive phases, following the line...

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[Incontinentia pigmenti].

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ژورنال

عنوان ژورنال: Güncel retina

سال: 2023

ISSN: ['2564-7156', '2548-0693']

DOI: https://doi.org/10.37783/crj-0360