[Home ] [Archive]    
:: Main About journal Editorial Board Current Issue Archive Submit an article Site Map Contact ::
:: Volume 7, Issue 1 (3-2018) ::
Int J Med Invest 2018, 7(1): 0-0 Back to browse issues page
Primary Growth Hormone Deficiency And Usher Syndrome: A Case Report
Reza Jafari , Banafshe Nouri *
Abstract:   (1737 Views)
Introduction: The Usher syndrome (USH) is an autosomal-recessive disorder refers to The combinded bilateral sensorineural hearing loss, retinitis pigmentosa (RP), and in some cases vestibular dysfunction. There are three clinical types of Usher syndrome: type 1, type 2, and type 3. Type 3 is characterised by progressive hearing loss and variable age of onset of retinal degenerationand he or she will usually require hearing aids by mid- to late adulthood. Night blindness usually begins sometime during puberty. Case Presentation: The present case reports is a 13 years-old male with type 3 of usher syndrome syndrome who developed a previously undescribed growth hormone de- ficiency. Conclusion: We sugesst usher syndrome type 3 could be a primery GH deficiency disorders.potential link between usher syndrome and GH deficiency is still unclear and needs further studies.
Keywords: Usher syndrome, GH deficiency, Retinitis pigmentosa
Full-Text [PDF 395 kb]   (481 Downloads)    
Type of Study: case report | Subject: General
Add your comments about this article
Your username or Email:

CAPTCHA code


XML     Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Jafari R, Nouri B. Primary Growth Hormone Deficiency And Usher Syndrome: A Case Report. Int J Med Invest. 2018; 7 (1)
URL: http://intjmi.com/article-1-301-en.html


Volume 7, Issue 1 (3-2018) Back to browse issues page
International Journal of Medical Investigation
Persian site map - English site map - Created in 0.05 seconds with 31 queries by YEKTAWEB 3815