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جلد 7 شماره 1 صفحات 0-0 برگشت به فهرست نسخه ها
Primary Growth Hormone Deficiency And Usher Syndrome: A Case Report
چکیده:   (1738 مشاهده)
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.
     
نوع مطالعه: گزارش مورد | موضوع مقاله: عمومى
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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-fa.html

Primary Growth Hormone Deficiency And Usher Syndrome: A Case Report. . 1396; 7 (1)

URL: http://intjmi.com/article-1-301-fa.html



دوره 7، شماره 1 - ( 12-1396 ) برگشت به فهرست نسخه ها
International Journal of Medical Investigation
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