Post - axial polydactyly in four limbs with different bony configurations

نویسنده

  • Rudrajit PAUL
چکیده

Polydactyly is a common congenital digital variation of the hand and foot, which is characterized by supernumerary digits. This condition can occur in one limb or can be exceptionally present in all four limbs; a condition called tetrapolydactyly. It may appear as isolated or in association with other birth defects. Polydactyly might be pre-axial, postaxial and central type, the post-axial being the commonest one [1]. Previously, occurrence of polydactyly was explained as the consequence of the failure of programmed cell death during fetal limb development. Early theories for polydactyly concerned disorders were programmed cell death cycle of fetal limb development. But now, specific genetic malfunctions are thought responsible. Hexadactyly of all the four limbs is a very rare skeletal malformation. Wollina et al. described such a case of pure post-axial polydactyly involving all the four limbs but no radiological investigation was possible in that case [2]. Surgical intervention in polydactyly are indicated for various reasons. To have a successful surgical procedure detailed knowledge regarding the bony architecture of the region is necessary. We here present a case of polydactyly involving all the four limbs where bony architecture is grossly different in the different limbs, knowledge of which will help the surgeons to plan the different surgical procedures. Case Report

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

In Response to the Article “Joubert Syndrome Imaging Features and Illustration of a Case”; Pol J Radiol, 2015; 80: 381–83

Joubert's syndrome is indeed a rarity in clinical and radiological practice with a myriad of accompanying anomalies. Figure 1. Clinical photos of the patient showing post-axial polydactyly in the upper and lower limbs (A, B) and broad flat nasal bridge (C). Herein we present a case of an eight-month-old female infant who presented with delayed milestones, nystagmus and post-axial polydactyly (F...

متن کامل

Five-fingered hand associated with partial or complete tibial absence and pre-axial polydactyly. A kindred of 15 affected individuals in five generations.

A kindred of 15 affected individuals in five generations is described with autosomal dominant inheritance of bilateral five-fingered hand. Some of them had additional pre-axial polydactyly of the fingers or toes and some had partial or complete absence of the tibia. The range of expression of the gene is variable and genetic advice to these families must take account of the whole spectrum of de...

متن کامل

Decision-making and Management of Ulnar Polydactyly of the Newborn: Outcomes and Satisfaction.

BACKGROUND Polydactyly is the most common congenital hand deformity. There is currently no consensus among pediatricians or hand surgeons regarding optimal management of ulnar (post-axial) type B polydactyly leading to uncertainty in initial treatment decisions for infants with this type of deformity. METHODS Parents of newborns with type B ulnar polydactyly were enrolled in a prospective, no...

متن کامل

Polydactyly: phenotypes, genetics and classification

Polydactyly is one of the most common hereditary limb malformations featuring additional digits in hands and/or feet. It constituted the highest proportion among the congenital limb defects in various epidemiological surveys. Polydactyly, primarily presenting as an additional pre-axial or post-axial digit of autopod, is a highly heterogeneous condition and depicts broad interand intra-familial ...

متن کامل

Peters anomaly with post axial polydactyly, ocular hypertelorism, a low nasal bridge, retrognathia, undescended testis, microphthalmia, and club foot in an Indian neonate: A case report

A case of Peters anomaly with bilateral post axial polydactyly, convex soles, ocular hypertelorism, a low nasal bridge, retrognathia, undescended testis, microphthalmia and club foot was examined in a neonatal Indian baby girl who had been delivered in the hospital and admitted to the newborn unit. She died aged five days. There were no cases of Peters anomaly recorded in India according to a l...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2011