Are Consanguineous Marriages to Blame for Usher Syndrome Type 1, a Rare Disease in Pakistan?

Usher syndrome type I is a rare genetic autosomal recessive disease caused by mutations in specific genes that provide instructions for making proteins involved in normal hearing, vision, and balance. It is characterized by hearing impairment due to the inability of auditory nerves to send sensory i...

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Veröffentlicht in:	Curēus (Palo Alto, CA) CA), 2020-10, Vol.12 (10)
Hauptverfasser:	Awan, Ali I, Abdul Raffay, Eusha, Liaqat, Ayesha, Hassan, Taimoor, Khan, Maria
Format:	Artikel
Sprache:	eng
Schlagworte:	Genetics Ophthalmology Otolaryngology
Online-Zugang:	Volltext
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