𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Hearing loss in a family affected by Fabry disease

✍ Scribed by Bruno Sergi; Guido Conti

Publisher
Springer
Year
2007
Tongue
English
Weight
377 KB
Volume
30
Category
Article
ISSN
0141-8955

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Optic atrophy and sensorineural hearing
Optic atrophy and sensorineural hearing loss in a family caused by an R445H OPA1 mutation
✍ Chunmei Li; Gregory Kosmorsky; Kang Zhang; Bradley J. Katz; Jian Ge; Elias I. Tr πŸ“‚ Article πŸ“… 2005 πŸ› John Wiley and Sons 🌐 English βš– 120 KB πŸ‘ 1 views

## Abstract Autosomal dominant optic atrophy (ADOA) is the most common form of inherited optic atrophy. Four genetic loci have been associated with ADOA: OPA1, OPA2, OPA3, and OPA4. Out of these four loci, only one gene has been identified, __OPA1.__ We previously described a unique syndrome of opt

Sensorineural hearing loss in sickle cel
Sensorineural hearing loss in sickle cell diseaseβ€”A prospective study from Oman
✍ Muhammed Hesham Al Okbi; Salam Alkindi; Rashid K. Al Abri; John Mathew; Afarida πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons 🌐 English βš– 622 KB

## Abstract ## Background: Sickle cell disease (SCD) is characterized by intermittent episodes of vascular occlusion and end‐organ damage. Neurologic symptoms are frequent and auditory involvement is not unexpected. ## Aim: To study the prevalence and pattern of hearing loss in Omani patients wi