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Lymphedema–distichiasis syndrome: a distinct type of primary lymphedema caused by mutations in the FOXC2 gene

✍ Scribed by Maaike Vreeburg; Martijn V. Heitink; Robert J. Damstra; Ute Moog; Michel Van Geel; Maurice A. M. Van Steensel


Book ID
110878565
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
772 KB
Volume
47
Category
Article
ISSN
0011-9059

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## Abstract Signs of neurofibromatosis type 1 (NF1) and Noonan syndrome (NS), two distinct autosomal dominant disorders, occur together in patients reported as Watson syndrome (WS), neurofibromatosis‐Noonan syndrome (NFNS), partial LEOPARD syndrome, NS with features of NF1, and NF1 with Noonan‐like