The de Barsy Syndrome
Küçük Resim Yok
Tarih
2001
Yazarlar
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
TURKISH J PEDIATRICS
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
We report a child with de Barsy syndrome, which is a very rare, genetically transmitted clinical entity associated with mental and growth retardation, severe cutis laxa, joint laxity and various ocular and skeletal system findings. The patient was operated to treat her orthopedic disabilities. Typical findings of this case with eight-year follow-up beginning from birth are described and compared with previously reported cases. The main aim of this paper was to describe the diagnostic and therapeutic difficulties of this rarely encountered syndrome.
Açıklama
Anahtar Kelimeler
de Barsy syndrome, hypermobility, elastin, cutis laxa, children
Kaynak
Turkish Journal of Pediatrics
WoS Q Değeri
Q4
Scopus Q Değeri
Q3
Cilt
43
Sayı
1
Künye
Arazi, M., Kapıcıoğlu, M. I. S., Mutlu, M., (2001). The de Barsy Syndrome. Turkish Journal of Pediatrics, 43(1), 79-84.
