Affiliation:
1. Health College of Pernambuco, Brazil
2. Federal University of Pernambuco; Hospital Cancer Pernambuco; Institute of Medicine Professor Fernando Figueira; Hospital Otavio de Freitas
Abstract
The De Sanctis-Cacchione Syndrome is the rarest and most severe kind of xeroderma pigmentosum, characterized by microcephaly, hypogonadism, neurological disorders, mental and growth retardation, with very few cases published. The clinical findings compatible with De Sanctis-Cacchione Syndrome and the therapeutic approach used to treat a one year and nine months old child, with previous diagnosis of xeroderma pigmentosum, are reported.
Reference10 articles.
1. Xeroderma pigmentoso con retraso psicomotor: síndrome de De Sanctis Cacchione. Reporte de 2 casos de origen mexicano;Liy MDC;Dermatol Pediatr Lat,2004
2. Anestesia em paciente com Xeroderma Pigmentoso: relato de caso;Oliveira CRD;Rev Bras Anestesiol,2000
3. Xeroderma pigmentoso. Síndrome de Sanctis Cacchione: Presentación de 1 caso;Falcón Lincheta L;Rev Cubana Pediatr,1998
4. Xeroderma Pigmentosum: cutaneous, ocular, and neurologic abnormalities in 830 published cases;Kraemer KH;Arch Dermatol,1987
5. The role of dermabrasion and chemical peels in the treatment of patients with xeroderma pigmentosum;Nelson BR;J Am Acad Dermatol,1995
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