نتایج جستجو برای: deafness kid syndrome

تعداد نتایج: 628914  

ابوالفضلی, محمدرضا, علی زاده, لیلا,

Long QT syndrome, which is defined by corrected QT interval longer than 0.45 seconds in men and o. 47 sec in women , could be divided into idiopathic (congenital ) and acquired forms. The idiopathic form is a familial disorder that can be associated with sensorineural deafness (Jervell and Lange- Neelson syndrome), which is transmitted with an autosomal recessive pattern. Although this syndrome...

2003
Gisele Viana de Oliveira Carlos Eduardo Steiner Maria Letícia Cintra Antonia Paula Marques-de-Faria

We report on a 22-year-old male patient and his father, both presenting with congenital sensorineural deafness, diffuse palmoplantar keratoderma and knuckle pads. These findings are similar to those previously described in the Bart-Pumphrey syndrome, a rare autosomal dominant disorder. Several conditions including keratoderma and deafness are briefly reviewed.

2013
A Insalaco G Prencipe PS Buonuomo I Ceccherini C Bracaglia M Pardeo R Nicolai F De Benedetti

Introduction Cryopyrin-associated periodic syndrome (CAPS) is an autoinflammatory syndrome caused by heterozygous mutations of CIAS1/NLRP3 gene. Affected patients may present three different phenotypes: familial cold autoinflammatory syndrome (FCAS), Muckle-Wells syndrome and CINCA syndrome. Common symptoms include sporadic or cold-induced non pruritic urticarial rash and fever. Severe cases su...

2016
Penghui Chen Longxia He Xiuhong Pang Xiaowen Wang Tao Yang Hao Wu

Nonsyndromic deafness is genetically heterogeneous but phenotypically similar among many cases. Though a variety of targeted next-generation sequencing (NGS) panels has been recently developed to facilitate genetic screening of nonsyndromic deafness, some syndromic deafness genes outside the panels may lead to clinical phenotypes similar to nonsyndromic deafness. In this study, we performed com...

2000
S Van Doornum

Cogan’s syndrome is a rare, multisystem disease which occurs predominantly in children and young adults. It was originally described as the combination of interstitial keratitis and audiovestibular disturbance, but other forms of ocular disease, as well as systemic vasculitis, have since been recognised as part of the syndrome. Diagnosis can be diYcult if the various manifestations occur separa...

2014
José MARTÍNEZ Jordi VALOR ABAD

The goal of this paper is to present Yabloesque versions of Grelling’s and Zwicker’s paradoxes concerning the notions of “heterological” and “hypergame” respectively. We will offer counterparts of these paradoxes that do not seem to involve self-reference or vicious circularity.

2017
Christine Neuhaus Tobias Eisenberger Christian Decker Sandra Nagl Cornelia Blank Markus Pfister Ingo Kennerknecht Cornelie Müller-Hofstede Peter Charbel Issa Raoul Heller Bodo Beck Klaus Rüther Diana Mitter Klaus Rohrschneider Ute Steinhauer Heike M Korbmacher Dagmar Huhle Solaf M Elsayed Hesham M Taha Shahid M Baig Heidi Stöhr Markus Preising Susanne Markus Fabian Moeller Birgit Lorenz Kerstin Nagel-Wolfrum Arif O Khan Hanno J Bolz

BACKGROUND Combined retinal degeneration and sensorineural hearing impairment is mostly due to autosomal recessive Usher syndrome (USH1: congenital deafness, early retinitis pigmentosa (RP); USH2: progressive hearing impairment, RP). METHODS Sanger sequencing and NGS of 112 genes (Usher syndrome, nonsyndromic deafness, overlapping conditions), MLPA, and array-CGH were conducted in 138 patient...

2010
Cengiz Kara Mehtap Kılıç Ahmet Uçaktürk Murat Aydın

Pendred syndrome (PDS) is an autosomal recessive disorder characterized by congenital deafness, goiter and iodide organification defect. Presence of inner ear malformations is essential for the clinical diagnosis. Most individuals with PDS are clinically and biochemically euthyroid. Mutations in the PDS gene encoding pendrin protein have been shown to be associated with PDS. It has been recentl...

Journal: :Journal of the American Academy of Dermatology 2004
Jay R Montgomery Thomas W White Bryan L Martin Maria L Turner Steven M Holland

We report the case of a congenitally deaf white male with mild palmoplantar keratoderma, ichthyosiform scaling, follicular hyperkeratosis, and mild keratitis, features consistent with keratitis-ichthyosis-deafness syndrome. His major problem was severe, disfiguring, inflammatory dissecting folliculitis of the scalp, hidradenitis suppurativa, and cystic acne, features comprising the follicular o...

2017
Antigone Papavasiliou Katerina Foska John Ioannou Mato Nagel

BACKGROUND Epilepsy, ataxia, sensorineural deafness, tubulopathy syndrome is a multi-organ disorder that links to autosomal recessive mutations in the KCNJ10 gene, which encodes for the Kir4.1 potassium channel. It is mostly described in consanguineous, non-European families. CASE REPORT A European male of non-consanguineous birth, with early-onset, static ataxic motor disorder, intellectual ...

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