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Family caregivers{u2019} knowledge and practices among children with phenylketonuria : A suggests nursing care protocol / Rehab Fouad Abdelkodoos ; Supervised Effat Elkarmalawy , Laila Kamal Eldin Effat , Heba Magdy Sharaa

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Rehab Fouad Abdelkodoos , 2018Description: 219 , 18 Leaves : charts , facsimiles , photographs ; 30cmOther title:
  • معلومات وممارسات مقدمى الرعاية الصحية الأسرية لأطفال الفنيل كيتونيوريا : بروتكول رعاية تمريضية مقترح [Added title page title]
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  • Issued also as CD
Dissertation note: Thesis (Ph.D.) - Cairo University - Faculty of Nursing - Department of Community Health Nursing Summary: PKU is an inherited disorder in which the body lacks the enzyme needed to convert Phe to tyrosine. Excess Phe accumulates in the blood and tissues can damage the brain and nervous system if left untreated (Didycz & Bik-Multanowski, 2018). PKU disease is the most common chronic genetic disorder which needs family caregivers' daily effort to deal with the child's disabilities, maintain a special rehabilitation and diet program, monitoring blood Phe level and child{u2019}s growth; and coping with such needs may be difficult. Maintaining long time nutrition regimens and applying complementary diets are the main therapeutic tasks in treating children with PKU which require perfect collaboration of the family caregivers (Regnault et al., 2015)
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Item type Current library Home library Call number Copy number Status Date due Barcode
Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.17.01.Ph.D.2018.Re.F (Browse shelf(Opens below)) Not for loan 01010110076608000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.17.01.Ph.D.2018.Re.F (Browse shelf(Opens below)) 76608.CD Not for loan 01020110076608000

Thesis (Ph.D.) - Cairo University - Faculty of Nursing - Department of Community Health Nursing

PKU is an inherited disorder in which the body lacks the enzyme needed to convert Phe to tyrosine. Excess Phe accumulates in the blood and tissues can damage the brain and nervous system if left untreated (Didycz & Bik-Multanowski, 2018). PKU disease is the most common chronic genetic disorder which needs family caregivers' daily effort to deal with the child's disabilities, maintain a special rehabilitation and diet program, monitoring blood Phe level and child{u2019}s growth; and coping with such needs may be difficult. Maintaining long time nutrition regimens and applying complementary diets are the main therapeutic tasks in treating children with PKU which require perfect collaboration of the family caregivers (Regnault et al., 2015)

Issued also as CD

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