De Sanctis-Cacchione Syndrome in a female infant - Case report
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 th...
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| Main Authors: | , |
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| Format: | Book |
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Sociedade Brasileira de Dermatologia,
2013-12-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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| Summary: | 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. |
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| Item Description: | 0365-0596 10.1590/abd1806-4841.20132844 |