Thanatophoric Dysplasia Detected During Prenatal Period
Öz
Thanatophoric dysplasia is one of the
newborn’s dwarfism syndromes usually resulting in death during perinatal period
and manifesting as short extremities. It is characterized by macrocephaly,
prominent forehead, narrow thorax, short extremities, flattened vertebral
bodies, curved femurs. This is caused by mutations in the fibroblast growth
factor receptor 3 (FGFR3) gene and
shows autosomal dominant inheritance model. In this report, we presented a case
with abnormal USG findings during perinatal period and detected to carry a
p.R248C mutation in FGFR3 gene in
amniosynthesis fluid.
Anahtar Kelimeler
Kaynakça
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- Referans2 Dighe M, Fligner C, Cheng E, Warren B, Dubinsky T. Fetal skeletal dysplasia: an approach to diagnosis with illustrative cases. Radiographics 2008;28:1061.
- Referans3 Orioli IM, Castilla EE, Barbosa-Neto JG. The birth prevalence rates for the skeletal dysplasias. J Med Genet 1986;23:328–32.
- Referans4 Martínez-Frías ML, Ramos-Arroyo MA, Salvador J. Thanatophoric dysplasia: an autosomal dominant condition?. Am J Med Genet 1988;31:815-20.
- Referans5 Wilcox WR, Tavormina PL, Krakow D, et al. Molecular, radiologic, and histopathologic correlations in thanatophoric dysplasia. Am J Med Genet 1998;78:274-81.
- Referans6 Hatzaki A, Sifakis S, Apostolopoulou D, et al. FGFR3 related skeletal dysplasias diagnosed prenatally by ultrasonography and molecular analysis: Presentation of 17 cases. Am J Med Genet Part A 2011;155:2426–35.
- Referans7 Baker KM, Olson DS, Harding CO, Pauli RM. Long term survival in typical thanatophoric dysplasia type 1. Am J Med Genet 1997;70:427-36.
- Referans8 Langer LO, Yang SS, Hall JG, et al. Thanatophoric dysplasia and cloverleaf skull. Am J Med Genet 1987;3:167–79.
Ayrıntılar
Birincil Dil
Türkçe
Konular
-
Bölüm
Olgu Sunumu
Yazarlar
Hande Özkalaycı
Bu kişi benim
Murat Celiloğlu
Bu kişi benim
Derya Erçal
Bu kişi benim
Elçin Bora
Bu kişi benim
Yayımlanma Tarihi
17 Aralık 2017
Gönderilme Tarihi
27 Ocak 2017
Kabul Tarihi
24 Mayıs 2017
Yayımlandığı Sayı
Yıl 2017 Cilt: 31 Sayı: 3