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Sturge–Weber syndrome in a 6-year-old girl
Penulis
: D. E. C. PEREZ, J. S. PEREIRA NETO, E. GRANER, & M. A. LOPES
Edisi
: 15
Editor
:
Collation
:
Subyek
:
Penerbit
: Paediatric Dentistry
Tahun
: 2005
ISBN
:
Call Number
:
Ringkasan :
Sturge–Weber syndrome (SWS), or encephalotrigeminal angiomatosis, is a rare, non-hereditary condition characterized by a facial cutaneous vascular nevus (nevus flammeus or port wine stain) in association with leptomeningeal angiomatosis [1,2].

Daftar copy :
No. Barcode Lokasi No. Rak Ketersediaan
1 08195158 Ruang Referensi - Perpustakaan FKIK 01 TIDAK DIPINJAMKAN

 

Diproses dalam : 0.14462494850159 detik
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