[Clinical features and genetics of the ichthyosis vulgaris group].
作者信息
Traupe H, Happle R
出版信息
Fortschr Med. 1980 Dec 11;98(46):1809-15.
PMID:7274918
Abstract
Combined application of clinical, genetic and histological criteria in general allows a definite diagnosis of autosomal dominant ichthyosis vulgaris and of X-linked recessive ichthyosis. For differential diagnosis, the following rare syndromes should be considered: ichthyosis bullosa: Refsum syndrome; Jung-Vogel syndrome; ichthyosis with corneal opacity, pili torti and alopecia; ichthyosis with deafness, pili torti and dental anomalies; and ichthyosis with hepatosplenomegaly and cerebellar degeneration.
摘要
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