Multipl konjenital anomalilerin eşlik ettiği nadir bir fasiyal asimetri olgusu
Öz
Anahtar Kelimeler
Kaynakça
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- Bawle EV, Conard J, Van Dyke DL, Czarnecki P, Driscoll DA. Seven new cases of Cayler cardiofacial syndrome with chromosome 22q11.2 deletion, including a familial case. Am J Med Genet 1998; 79: 406-10.
- Wright EM, O'Connor R, Kerr BA. Radial aplasia in CHARGE syndrome: a new association. Eur J Med Genet 2009; 52: 239-41.
- Stoll C, Viville B, Treisser A, Gasser B. A family with dominant oculoauriculovertebral spectrum. Am J Med Genet 1998; 78: 345-9.
- Joyce CA, Sharp A, Walker JM, Bullman H, Temple IK. Duplication of 7p12.1- p13, including GRB10 and IGFBP1, in a mother and daughter with features of Silver-Russell syndrome. Hum Genet 1999; 105: 273-80.
- Bonar BE, Owens RW. Bilateral congenital facial paralysis: review of the literature and a classification. Am J Dis Child 1929; 38: 1256-72.
- Pape KE, Pickering D. Asymmetric crying facies: an index of other congenital anomalies. J Pediatr 1972; 81: 21-30.
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Ayrıntılar
Birincil Dil
Türkçe
Konular
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Bölüm
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Yazarlar
Ayşegül Zenciroğlu
Ayşe Aksoy
Ramiz Gündüz
Yayımlanma Tarihi
20 Haziran 2011
Gönderilme Tarihi
26 Mayıs 2010
Kabul Tarihi
-
Yayımlandığı Sayı
Yıl 2011 Cilt: 33 Sayı: 2