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Report of a case of Zimmermann–Laband syndrome with new manifestations

✍ Scribed by Z. Lin; T. Wang; G. Sun; X. Huang

Book ID
116561988
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
533 KB
Volume
39
Category
Article
ISSN
0901-5027

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Zimmermann-Laband syndrome (ZLS) is characterised by findings of coarse facial appearance, hepatosplenomegaly, and hirsutism often first observed in infancy, followed by the evolution during childhood of gingival fibromatosis, small joint hyperextensibility, and hypoplasia of the finger-and toenails