نتایج جستجو برای: radial polydactyly

تعداد نتایج: 62619  

Journal: :The Turkish journal of pediatrics 2003
Münevver Türkmen Kübra Temoçin Cağlar Acar Edi Levi Can Karaman Gülten Inan Nursel Elçioğlu

Short rib-polydactyly syndrome (SRPS) is a group of rare, lethal skeletal dysplasias characterized by short ribs and limbs, polydactyly, hypoplastic thorax and visceral anomalies. Our case had coarsening of facial features, low-set ears, lobulated tongue, cleft palate, and hypoplastic epiglottis. Short proximal parts of upper limbs, bilateral postaxial polydactyly of hands, and bifid big toe wi...

2017
Mario I Escudero Klaus Seebach Selene G Parekh Manuel J Pellegrini

INTRODUCTION Polydactyly is the most common congenital foot anomaly and consists of partial or complete duplication of a toe. Traditionally, surgical treatment has been amputation. There is little evidence when surgical treatment requires repairing the stabilizing structures of the metatarsophalangeal joint. OBJECTIVE Assess the functional and radiologic outcomes of a case of postaxial polyda...

2014
Sampat Dumbre Patil Hemant Parekh Vaishali Dumbre Patil Kartikeya Joshi

INTRODUCTION Congenital hallux varus of secondary type is associated with polydactyly, syndactyly or other congenital deformities of the foot. Such congenital deformities can be addressed in childhood with soft tissue reconstructive procedures. In adulthood, treatment of these deformities is challenging because of soft tissue contractures and rigid bony deformities. To our knowledge, this is th...

Journal: :Journal of medical genetics 1997
T Sasaki H Tonoki H Soejima N Niikawa

We report on an 11 year old girl with trichorhinophalangeal syndrome type I (TRPS1), postaxial polydactyly of the fingers, and a de novo paracentric inversion on the long arm of chromosome 8 involving bands q13.1 and q24.11. Molecular analysis using FISH and polymorphic DNA markers detected an approximately 4 Mb, cytogenetically unidentified deletion occurring between two STSs markers, AFMB331Y...

Journal: :Development 2003
Ottheinz Krebs Claire M Schreiner William J Scott Sheila M Bell David J Robbins John A Goetz Heidi Alt Norm Hawes Eckhard Wolf Jack Favor

A unique limb phenotype is described in a radiation-induced mutant mouse resulting from an inversion of a proximal segment of chromosome 5. The limb phenotype in the homozygous mutant presents with two anterior skeletal elements in the zeugopod but no posterior bone, hence the name replicated anterior zeugopod, raz. The zeugopod phenotype is accompanied by symmetrical central polydactyly of han...

Journal: :Developmental period medicine 2016
Agnieszka Szmigielska Grażyna Krzemień Maria Roszkowska-Blaim Ewa Obersztyn

UNLABELLED The prevalence of obesity in children is still rising all over the world. The most common reason for significant weight gain is a high-calorie diet and decreased physical activity. However, apart from environmental factors, genetic predisposition plays a crucial role in the pathomechanism of obesity. We present the case of a boy with pathological obesity and Bardet-Biedl syndrome (BB...

Journal: :Journal of Korean Medical Science 1998
N. H. Myong J. W. Park J. G. Chi

Short rib-polydactyly syndrome (SRPS) is a group of lethal skeletal dysplasia of an autosomal recessive inheritance characterized by markedly narrow ribs, micromelia, and multiple anomalies of major organs. We report a case of type IV SRPS with uncommon associations of polydactyly and bilateral polycystic kidneys, in a 28 week old female fetus. She was born dead to a 28 year old mother, showing...

Journal: :Pediatric Traumatology, Orthopaedics and Reconstructive Surgery 2015

Journal: :International Journal of Molecular Sciences 2021

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