Demirhan sydrome, a new sydrome: Fibular agenesis, cleft palate, absence of multiple permanent teeth and labial hypoplasia

Autor: Demirhan O., Mungan N.O., Toroglu S., Binokay F., Taştemir D., Solgun H.A.
Přispěvatelé: Çukurova Üniversitesi
Jazyk: angličtina
Rok vydání: 2008
Předmět:
Popis: Background: There are some syndromes described in the literature with agenesis of fibulae and tibia, but to the best of our knowledge, our case is the first one defined with fibular agenesis, and tibial bowing without involvement of femur or upper extremity deformities and teeth abnormalities. Case Report: We report a twelve years old girl, who had severe growth retardation, major lower extremity abnormalities, torticollis, flat face, hypertelorism, thin upper lip, displaced teeth, cleft palate, and labial hypoplasia. Chromosome analysis was performed. Her karyotype was normal female (46,XX) and no chromosomal abnormality was detected. Conclusions: The clinical findings of this case is not in accordance with any known syndrome. It is a new syndrome according to our opinion. © The American Journal of Case Report.
Databáze: OpenAIRE