نتایج جستجو برای: nonsyndromic

تعداد نتایج: 1750  

2012
Laura M Dominguez Kelley M Dodson

The purpose of this review is to assess the current literature on deafness nonsyndromic autosomal dominant 2 (DFNA2) hearing loss and the mutations linked to this disorder. Hearing impairment, particularly nonsyndromic hearing loss, affects multiple families across the world. After the identification of the DFNA2 locus on chromosome 1p34, multiple pathogenic mutations in two genes (GJB3 and KCN...

2017
Humayun Ahmed Hossein Akbari Abdolhasan Emami Mohammad R. Akbari

Syndactyly and polydactyly-respectively characterized by fused and supernumerary digits-are among the most common congenital limb malformations, with syndactyly presenting at an estimated incidence of 1 in 2,000-3,000 live births and polydactyly at a frequency of 1 in approximately 700-1,000 live births. Despite their relatively regular manifestation in the clinic, the etiologies of syndactyly ...

Journal: :American journal of human genetics 2013
Anne-Karin Arndt Sebastian Schafer Jorg-Detlef Drenckhahn M Khaled Sabeh Eva R Plovie Almuth Caliebe Eva Klopocki Gabriel Musso Andreas A Werdich Hermann Kalwa Matthias Heinig Robert F Padera Katharina Wassilew Julia Bluhm Christine Harnack Janine Martitz Paul J Barton Matthias Greutmann Felix Berger Norbert Hubner Reiner Siebert Hans-Heiner Kramer Stuart A Cook Calum A MacRae Sabine Klaassen

Deletion 1p36 syndrome is recognized as the most common terminal deletion syndrome. Here, we describe the loss of a gene within the deletion that is responsible for the cardiomyopathy associated with monosomy 1p36, and we confirm its role in nonsyndromic left ventricular noncompaction cardiomyopathy (LVNC) and dilated cardiomyopathy (DCM). With our own data and publically available data from ar...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2009
Martin Schwander Wei Xiong Joshua Tokita Andrea Lelli Heather M Elledge Piotr Kazmierczak Anna Sczaniecka Anand Kolatkar Tim Wiltshire Peter Kuhn Jeffrey R Holt Bechara Kachar Lisa Tarantino Ulrich Müller

Deafness is the most common form of sensory impairment in humans and is frequently caused by single gene mutations. Interestingly, different mutations in a gene can cause syndromic and nonsyndromic forms of deafness, as well as progressive and age-related hearing loss. We provide here an explanation for the phenotypic variability associated with mutations in the cadherin 23 gene (CDH23). CDH23 ...

Journal: :Pediatric neurology briefs 2015
Wenjuan Chen Hongjie Yuan

Investigators from Yokohama City University and other medical centers in Israel and Japan reported mutations on N-methyl-D-aspartate (NMDA) receptors subunit GRIN1 (GluN1) identified in patients with nonsyndromic intellectual disability and early-onset epileptic encephalopathy.

Journal: :International Journal of Medical and Dental Case Reports 2018

Journal: :Journal of the American College of Cardiology 2016

Journal: :trauma monthly 0
hamed kermani department of oral and maxillofacial surgery, oral and maxillofacial diseases research center, school of dentistry, mashhad university of medical sciences, mashhad, ir iran nima dehghani department of oral and maxillofacial surgery, school of dentistry, kermanshah university of medical sciences, kermanshah, ir iran farzad aghdashi department of oral and maxillofacial surgery, school of dentistry, shahid beheshti university of medical sciences, tehran, ir iran mohammad esmaeelinejad department of oral and maxillofacial surgery, school of dentistry, shahid beheshti university of medical sciences, tehran, ir iran; department of oral and maxillofacial surgery, school of dentistry, shahid beheshti university of medical sciences, tehran, ir iran. tel: +98-2166050480, fax: +98-2122439976

conclusions physicians should be aware of the signs and symptoms of different pain sources to prevent misdiagnosis and maltreatment. introduction fracture of the styloid process (sp) of the temporal bone is a rare traumatic injury in normal individuals who are not suffering from eagle’s syndrome. diagnosis and management of this problem requires comprehensive knowledge about its signs and sympt...

2012
Seema Gupta Mridula Goswami

The apparently morphologically normal finding of multiple supernumerary teeth in absence of an associated systemic condition or syndrome is an uncommon phenomenon. Surgical removal of supernumerary teeth is indicated if eruption of the adjacent teeth has been delayed; altered eruption, displacement of adjacent teeth is evident or pathologies such as cystic lesion and resorption of adjacent toot...

2017
Dong Hwi Kim Hyo Sun Ko Young Joon Jun

Basal cell carcinoma (BCC) comprising several lesions is not uncommon, but nonsyndromic multiple BCCs with parotid invasion are rare entities. We present two cases of multiple sporadic, nonsyndromic BCCs, and one of these cases is a unique case of parotid invasion associated purely with actinic keratosis. In Case 1, a 79-year-old female presented with multiple skin lesions on the face and left ...

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