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Clinical spectrum of steroid sulfatase deficiency: X-linked recessive ichthyosis, birth complications and cryptorchidism

โœ Scribed by H. Traupe; R. Happle


Publisher
Springer
Year
1983
Tongue
English
Weight
418 KB
Volume
140
Category
Article
ISSN
0340-6997

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## Abstract We observed a boy with short stature, chondrodysplasia punctata, ichthyosis, and a terminal deletion of Xp. Steroid sulfatase deficiency was demonstrated in the patient's fibroblasts. Molecular analysis showed a deletion of the entire steroid sulfatase gene. This case represents another