نتایج جستجو برای: deafness kid syndrome

تعداد نتایج: 628914  

Journal: :The Turkish journal of pediatrics 2004
Ergun Cetinkaya Nazlihan Günal Nilgün Sönmez Zehra Aycan Sadi Vidinlisan Oz Kahramanyol Ilhan Paşaoğlu

The LEOPARD syndrome is a rare, autosomal dominant multisystemic disorder characterized by lentiginosis, ocular hypertelorism, abnormal genitalia, growth retardation, sensorineural deafness, and cardiac and electrocardiographic abnormalities. Although it is not cited, hypertrophic cardiomyopathy is often associated with the disease. In this study, we present a nine-year-old boy with LEOPARD syn...

2013
I Melki K Lambot L Jonard V Couloigner P Quartier B Neven B Bader-Meunier

Introduction Germline mutations in SLC29A3 result in a range of clinically related, recessive syndromes: H syndrome, pigmented hypertrichosis with insulin-dependent diabetes mellitus (PHID) syndrome, Faisalabad histiocytosis (FHC), and sinus histiocytosis with massive lymphadenopathy (SHML). Main symptoms of these diseases are hyperpigmentation with hypertrichosis, sensorineural deafness, diabe...

Journal: :South African Journal of Child Health 2014

Journal: :genetics in the 3rd millennium 0
سمیرا یادگاری samira yadegari department of neurology, shariati hospital, tehran university of medical sciences, tehran, iran شهریار نفیسی shahriar nafissi

brown-vialetto-van laere syndrome (bvvls) is a rare neurological disorder of unknown etiology considered to be a form of motor neuron diseases. this syndrome is characterized by bilateral deafness and involvement of lower cranial nerves, especially 7th-12th. umn signs are less frequent. until 2007, only fifty eight cases were reported. half of the reported cases were sporadic. in the remaining ...

Journal: :Journal of medical genetics 1990
S J Charles A T Moore J R Yates T Green P Clark

We report a case of Alstrom's syndrome with hypothyroidism in addition to the cardinal features of blindness, deafness, obesity, and insulin dependent diabetes mellitus. The parents were first cousins once removed which strengthens the case for autosomal recessive inheritance.

Ali Alesheykh Aliasghar Raouf Kiamarz Navia Masoud Khaki Mohammad Reza Sedaghat Morteza Mazloom Farsi Baf Ramin Zojaji,

Introduction: Pseudoexfoliation syndrome (PXS) occurs due to the deposition of extracellular fibrillar materials on the anterior chamber of the eye. This syndrome has been considered to be part of a systemic disease with the potential involvement of the inner ear called sensoroneural hearing loss (SNHL).  In this study, we aimed on evaluating SNHL within PXS patients in Iran to compare them wi...

2014
Philippe M Campeau Dalia Kasperaviciute James T Lu Lindsay C Burrage Choel Kim Mutsuki Hori Berkley R Powell Fiona Stewart Têmis Maria Félix Jenneke van den Ende Marzena Wisniewska Hülya Kayserili Patrick Rump Sheela Nampoothiri Salim Aftimos Antje Mey Lal D V Nair Michael L Begleiter Isabelle De Bie Girish Meenakshi Mitzi L Murray Gabriela M Repetto Mahin Golabi Edward Blair Alison Male Fabienne Giuliano Ariana Kariminejad William G Newman Sanjeev S Bhaskar Jonathan E Dickerson Bronwyn Kerr Siddharth Banka Jacques C Giltay Dagmar Wieczorek Anna Tostevin Joanna Wiszniewska Sau Wai Cheung Raoul C Hennekam Richard A Gibbs Brendan H Lee Sanjay M Sisodiya

BACKGROUND Deafness, onychodystrophy, osteodystrophy, mental retardation, and seizures (DOORS) syndrome is a rare autosomal recessive disorder of unknown cause. We aimed to identify the genetic basis of this syndrome by sequencing most coding exons in affected individuals. METHODS Through a search of available case studies and communication with collaborators, we identified families that incl...

Journal: :Bulletin de la Societe belge d'ophtalmologie 2001
K Van den Abeele M Craen J Schuil F M Meire

The Alström syndrome is a rare autosomal recessive disorder characterized by pigmentary retinopathy, diabetes mellitus, sensorineural deafness and obesity. A normal intelligence is often present. We report 9 patients.

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