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Sindrom Barde-Bidlq i sindrom Lourensa-Muna - redkie autosomno-recessiwnye zabolewaniq, imeüschie shodnyj klinicheskij fenotip. Jeti sindromy harakterizuütsq progressiruüschimi priznakami, wklüchaq distrofiü konusno-sharowidnoj setchatki, ozhirenie i gipogonadizm u muzhchin. Dopolnitel'nye klinicheskie proqwleniq mogut wklüchat' nesposobnost' k obucheniü, anomalii pochek i polidaktiliü. Nesmotrq na shodstwo, sindromy Barde-Bidlq i Lourensa-Muna otlichaütsq nekotorymi klinicheskimi osobennostqmi. V ätoj knige opisano lechenie glaznyh proqwlenij sindroma Barde-Bidlq s pomosch'ü nowyh metodow…mehr

Produktbeschreibung
Sindrom Barde-Bidlq i sindrom Lourensa-Muna - redkie autosomno-recessiwnye zabolewaniq, imeüschie shodnyj klinicheskij fenotip. Jeti sindromy harakterizuütsq progressiruüschimi priznakami, wklüchaq distrofiü konusno-sharowidnoj setchatki, ozhirenie i gipogonadizm u muzhchin. Dopolnitel'nye klinicheskie proqwleniq mogut wklüchat' nesposobnost' k obucheniü, anomalii pochek i polidaktiliü. Nesmotrq na shodstwo, sindromy Barde-Bidlq i Lourensa-Muna otlichaütsq nekotorymi klinicheskimi osobennostqmi. V ätoj knige opisano lechenie glaznyh proqwlenij sindroma Barde-Bidlq s pomosch'ü nowyh metodow terapii, osnowannyh na dokazatel'stwah.Suschestwuüschie warianty lecheniq ne qwlqütsq lechebnymi, oni mogut pomoch' zamedlit' progressirowanie i sohranit' zrenie. Kombinaciq citikolina, qgod godzhi, koänzima Q10 i lüteina predstawlqet soboj mnogoobeschaüschij podhod k lecheniü degeneracii setchatki u pacientow s BBS, hotq dlq podtwerzhdeniq ih äffektiwnosti neobhodimy dal'nejshie klinicheskie ispytaniq.
Autorenporträt
Aamir Jalal Al-Mosawi is advisor doctor at the National Training and Development Center of the Iraqi Ministry of Health and Baghdad Medical City. He was the Head of Iraq Headquarter of Copernicus Scientists International Panel (2006-October, 2020). He is also member of the advisory council, the International Association of Medical Colleges (IAMC).