Photosensitivity, corneal scarring and developmental delay: Xeroderma Pigmentosum in a tropical country
نویسندگان
چکیده
We present the case of an 8 year-old girl in a developing country with significant corneal scarring and multiple cutaneous skin lesions in sun-exposed areas. Neuro-developmental delay had been present since 3 months of age, and taken as a whole the consensus was that this clinical picture was consistent with Xeroderma Pigmentosum (XP). We highlight the difficulties encountered due to the lack of diagnostic and treatment modalities for this child, and offer a brief review of XP, including emerging treatments that show potential.
منابع مشابه
Corneal Involvement in Xeroderma Pigmentosum;a Histopathologic Report
PURPOSE To report the histopathologic features of corneal involvement in a patient with xeroderma pigmentosum (XP). CASE REPORT A 19-year-old man with XP presented with bilateral corneal leukoma and decreased visual acuity predominatly in his right eye. Penetrating keratoplasty was performed in the right eye due to severe corneal opacity, vascularization and lipid deposition. The corneal butt...
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Xeroderma pigmentosum (XP) is a rare disorder, inherited as an autosomal recessive gemodermatosis. It is characterized by photosensitivity, freckly pigmented changes, premature skin ageing, telegiectasis, warty and papillomatous growth and malignant tumor development in later stage. It results from mutation in seven nucleotide excision repair gene (XP-A to XP-G complement groups) and post repli...
متن کاملXERODERMA PIGMENTOSUM WITH NEUROLOGICA L COMPLICATIONS: THE DESA NCTIS-CA CCHIONE SYNDROME
A 7 year old boy with DeSanctis-Cacchione syndrome - xeroderma pigmentosum, microcephaly, mental deficiency, dwarfism and gonadal hypoplasia - will be presented.
متن کاملXeroderma pigmentosum: a review and case series.
Xeroderma pigmentosa (XP) is a condition inherited as an autosomal recessive trait and is characterized by photosensitivity, pigmentary changes, premature skin ageing and malignant tumour development resulting from the defect in DNA repair. The management of complications of XP, especially orofacial tumours entails an enormous surgical challenge to the clinicians. We present five cases of XP.
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ورودعنوان ژورنال:
- Cases Journal
دوره 1 شماره
صفحات -
تاریخ انتشار 2008