𝔖 Bobbio Scriptorium
✦   LIBER   ✦

GJB2 mutations in patients with non-syndromic hearing loss from Northeastern Hungary

✍ Scribed by Tímea Tóth; Susan Kupka; Birgit Haack; Kathrin Riemann; Simone Braun; Ferenc Fazakas; Hans-Peter Zenner; László Muszbek; Nikolaus Blin; Markus Pfister; István Sziklai


Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
68 KB
Volume
23
Category
Article
ISSN
1059-7794

No coin nor oath required. For personal study only.

✦ Synopsis


Mutations in the GJB2 gene encoding the gap-junction protein connexin 26 have been identified in many patients with childhood hearing impairment (HI). One single mutation, c.35delG, accounts for the majority of mutations in Caucasian patients with HI. In the present study we screened 500 healthy control individuals and a group of patients with HI from Northeastern Hungary for GJB2 mutations. The patients' group consisted of 102 familial from 28 families and 92 non-familial cases. The most common mutation in the Hungarian population is the c.35delG, followed by the c.71G>A (p.W24X) mutation. 34.3% of the patients in the familial group were homozygous, and 17.6% heterozygous for 35delG. In the non-familial group the respective values were 37% and 18% (allele frequency: 46.2%). In the general population an allele frequency of 2.4% was determined. Several patients were identified with additional, already described or new GJB2 mutations, mostly in heterozygous state. The mutation c.380G>A (p.R127H) was formerly found only in heterozygous state and its disease relation was controversial. We demonstrated the presence of this mutation in a family with three homozygous patients and 4 heterozygous unaffected family members, a clear indication of recessively inherited HI. Furthermore, we provided evidence for the pathogenic role of two new mutations, c.51C>A (p.S17Y) and c.177G>T (p.G59V), detected in the present study. In the latter case the pattern of inheritance might be dominant. Our results confirm the importance of GJB2 mutations in the Hungarian population displaying mutation frequencies that are comparable with those in the Mediterranean area.


📜 SIMILAR VOLUMES


GJB2 mutations in Iranians with autosoma
✍ Hossein Najmabadi; Robert A. Cucci; Solmaz Sahebjam; Nafiseh Kouchakian; Mohamma 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 142 KB

Hereditary hearing loss (HHL) is an extremely common disorder. About 70% of HHL is non-syndromic, with autosomal recessive forms accounting for ~ 85% of the genetic load. Although very heterogeneous, the most common cause of HHL in many different world populations is mutations of GJB2, a gene that e

The 342-kb deletion in GJB6 is not prese
✍ Barbara Günther; Andrea Steiner; Doris Nekahm-Heis; Klaus Albegger; Patrick Zoro 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 26 KB

Recently, a 342-kb deletion involving GJB6 was associated with autosomal-recessive non-syndromic hearing loss (NSHL) and in combination with a GJB2 mutation with digenic NSHL. This deletion was the second most common mutation causing prelingual NSHL in Spain, and was frequently observed in patients

Frequencies of GJB2 mutations in German
✍ Susan Kupka; Simone Braun; Susanne Aberle; Birgit Haack; Margret Ebauer; Ulrike 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 197 KB

Mutations in the GJB2 gene encoding the gap-junction protein connexin 26 have been identified in many patients with childhood hearing impairment (HI). One single mutation, 35delG (30delG), accounts for up to 70% of all analyzed European patients with autosomal recessive inherited HI and 10% of patie

Mutations in the connexin26/GJB2 gene ar
✍ Heinz Gabriel; Petra Kupsch; Jürgen Sudendey; Elke Winterhager; Klaus Jahnke; Jü 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 68 KB

Congenital sensorineural hearing loss affects approximately 1/1,000 live births. Mutations in the gene encoding connexin26 (GJB2) have been described as a major cause of genetic nonsyndromic hearing impairment. Additionally, another gap junction gene, connexin30 (GJB6), was found to be responsible f