Rare case of tibial hemimelia, preaxial polydactyly, and club foot
نویسندگان
چکیده
منابع مشابه
Rare case of tibial hemimelia, preaxial polydactyly, and club foot
A seven-month old female presented with left tibial hemimelia (or congenital tibial aplasia; Weber type VIIb, Jones et al type 1a), seven-toed preaxial polydactyly, and severe club foot (congenital talipes equinovarus). Definitive amputation surgery disarticulated the lower limb at the knee. This case report describes the anatomical findings of a systematic post-amputation examination of the lo...
متن کاملPreaxial polydactyly of the foot
Background and purpose - Preaxial polydactyly of the foot is a rare malformation and clinicians are often unfamiliar with the associated malformations and syndromes. In order to give guidelines for diagnostics and referral to a clinical geneticist, we provide an overview of the presentation using a literature review and our own patient population. Patients and methods - The literature review wa...
متن کاملTibial hemimelia-split hand/foot syndrome with rare anomalies.
Fig. 1.Claw like deformity of both hands, right sided tibial hemimelia with hypoplastic three toed foot and a transverse cleft on planter side of left foot. Tibial hemimelia-split hand/foot syndrome (TH-SHFM) is a rare constellation of multiple congenital malformations which includes Ectrodactyly (Lobster claw deformity or Cleft hand/foot) with a wide range of phenotypes of absent tibia/tibial ...
متن کاملAn unusual case of preaxial polydactyly of the hand
Preaxial polydactyly is the most common duplication pattern in white and Asian populations (1). It is a congenital anomaly with a wide range of manifestations .Current classification do not have the capacity to classify all different types of radial polydactyly. We describe here a very rare and unusual case of bilateral preaxial polydactyly (triplication) in a woman and report the operations re...
متن کاملPreaxial Polydactyly of the Foot: Variable Expression of Trisomy 13 in a Case from Central Africa
Trisomy 13 is a chromosomal disorder characterized by a severe clinical picture of multiple congenital anomalies. We here describe the clinical and genetic features and prognosis observed in a newborn with trisomy 13 from Central Africa. He presented the rare feature of preaxial polydactyly of the feet.
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ژورنال
عنوان ژورنال: World Journal of Clinical Cases
سال: 2016
ISSN: 2307-8960
DOI: 10.12998/wjcc.v4.i12.401