Ocular manifestations of nephropathic cystinosi / Mohammed Gamal Eldin Fathallah ; Supervised Neveen Abdelmonem Soliman , Akmal Abdelmonem Rizk , Ahmed Mohamed Badr
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TextLanguage: English Publication details: Cairo : Mohammed Gamal Eldin Fathallah , 2014Description: 143 P. : charts , facsimiles ; 25cmOther title: - دراسة تأثر العين فى مرض السيستينوسيس الكلوى [Added title page title]
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قاعة الرسائل الجامعية - الدور الاول | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.28.Ph.D.2014.Mo.O (Browse shelf(Opens below)) | Not for loan | 01010110065396000 | ||
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مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.28.Ph.D.2014.Mo.O (Browse shelf(Opens below)) | 65396.CD | Not for loan | 01020110065396000 |
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| Cai01.11.28.Ph.D.2014.Mo.I The influence of immunoglobulin IgG Fc - receptor polymorphisms on susceptibility to guillain - barre{u00B4} syndrome / | Cai01.11.28.Ph.D.2014.Mo.L Left ventricular geometry and n-terminal pro- brain natriuretic peptide in Egyptian pediatric chronic renal insufficiency patients / | Cai01.11.28.Ph.D.2014.Mo.L Left ventricular geometry and n-terminal pro- brain natriuretic peptide in Egyptian pediatric chronic renal insufficiency patients / | Cai01.11.28.Ph.D.2014.Mo.O Ocular manifestations of nephropathic cystinosi / | Cai01.11.28.Ph.D.2014.Mo.O Ocular manifestations of nephropathic cystinosi / | Cai01.11.28.Ph.D.2014.Sh.C Citrin deficiency in Egyptian infants with cholestasis / | Cai01.11.28.Ph.D.2014.Sh.C Citrin deficiency in Egyptian infants with cholestasis / |
Thesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of Pediatrics
Background: Nephropathic cystinosis is a rare genetic disease characterized by accumulation of the amino acid cystine in lysosomes throughout the body. Ocular manifestations, particularly corneal cystine crystal formation, remain a major complication of nephropathic cystinosis.Conclusion: Anterior segment ocular manifestations of nephropathic cystinosis are more frequent than posterior segment involvement, being uniformly present in almost all patients beyond infancy. Topical cysteamine therapy is effective in depleting cystine crystals from the avascular cornea. Nevertheless, there is a pressing need for long-acting cysteamine eye drops to enhance patient compliance and improve outcome
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