نتایج جستجو برای: limb reduction defects

تعداد نتایج: 685084  

Journal: :Human molecular genetics 2003
Françoise Gofflot Carine Hars Françoise Illien Françoise Chevy Claude Wolf Jacques J Picard Charles Roux

Human disorders caused by inborn errors of cholesterol biosynthesis are characterized by dysmorphogenesis of multiple organs. This includes limb malformations that are observed at high frequency in some disorders, such as the Smith-Lemli-Opitz syndrome, indicating a pivotal role of cholesterol in limb morphogenesis. Recently, it has been demonstrated that cholesterol can modulate the activity o...

Journal: :Archivos argentinos de pediatria 2014
Rosalba Sevilla-Montoya Braulio Ríos-Flores Elsa Moreno-Verduzco Mauricio Domínguez-Castro Carlos I Rivera-Pedroza Dra Mónica Aguinaga-Ríos

UNLABELLED Adams Oliver syndrome (AOS) is a highly variable entity with terminal transverse limb defects (TTLD) and aplasia cutis congenita (ACC) with a wide phenotypic spectrum. Several inheritance models have been observed; the most severe phenotype has been related to an autosomal recessive (AR) pattern of inheritance. OBJECTIVE. To present a family with two half siblings with a severe pheno...

Journal: :Journal of oral medicine and oral surgery 2022

Background: A positive prenatal history of maternal fever has been found to express as a range defects in infants including limb reduction, central nervous system defects, facial dysmorphogenesis and foetal death. Oromandibular hypogenesis syndrome is rare spectrum congenital disorders characterised by malformations the tongue, mandible, maxilla limbs. They present sporadic cases with extremely...

2015
Jeffrey M Dicke Samantha L Piper Charles A Goldfarb

OBJECTIVE The standard obstetric ultrasound examination includes documentation of arms and legs. The purpose of this study is to review the efficacy of ultrasound for the detection of limb anomalies, the type and incidence of associated malformations and pregnancy outcomes. METHOD All cases of polydactyly (POD), abnormal hand position (AHP), limb reduction defects (LRD) and arthrogryposis (AR...

2014
Akihiko Muto Shingo Ikeda Martha E. Lopez-Burks Yutaka Kikuchi Anne L. Calof Arthur D. Lander Thomas F. Schilling Gregory S. Barsh

Haploinsufficiency for Nipbl, a cohesin loading protein, causes Cornelia de Lange Syndrome (CdLS), the most common "cohesinopathy". It has been proposed that the effects of Nipbl-haploinsufficiency result from disruption of long-range communication between DNA elements. Here we use zebrafish and mouse models of CdLS to examine how transcriptional changes caused by Nipbl deficiency give rise to ...

2016
Susmitha Bandi Rayidi Venkata Koteswara Rao Damalacheruvu Mukunda Reddy

INTRODUCTION Primary microvascular reconstruction of multiple defects is challenging particularly if it has to be simultaneous. In trauma cases, harvesting two independent free flaps from different sites is very time-consuming and adds to morbidity. To eliminate these disadvantages, we sought to find out a reliable alternative method of harvesting two independent free flaps based on the descend...

Journal: :Toxicological sciences : an official journal of the Society of Toxicology 2006
Sarah E Ali-Khan Barbara F Hales

Bioactive retinoids are potent limb teratogens, upregulating apoptosis, decreasing chondrogenesis, and producing limb-reduction defects. To target the origins of these effects, we examined gene expression changes in the developing murine limb after 3 h of culture with teratogenic concentrations of vitamin A. Embryonic day 12 CD-1 limbs were cultured in the absence or presence of vitamin A (reti...

Journal: :Development 1989
N A Brown C I Hoyle A McCarthy L Wolpert

We are studying the development of handedness, in particular the relationships between handed structures with bilateral symmetry, for example the limbs, and those with lateral asymmetry, such as the heart, lungs and gut. Asymmetric (unilateral) developmental limb abnormalities can be induced by chemical treatment of mouse embryos, either in utero by acetazolamide, or in culture by misonidazole....

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