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| Hermanski-Pudlak Syndrome | ||||||||||||||||||||||||
| 2 Diseases
& Disorders
/
2 Eye
Diseases, Hereditary
/
2
Albinism /
2 Albinism, Oculocutaneous / ► Hermanski-Pudlak Syndrome |
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| MeSH description: Syndrome characterized by the triad of oculocutaneous albinism, platelet storage pool deficiency, and lysosomal accumulation of ceroid lipofuscin. | ||||||||||||||||||||||||
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| ► Catalogue of Ophthalmic Journals | ||||||||||||||||||||||||
| Other Links | ||||||||||||||||||||||||
| ►
eMedicine:
Hermanski-Pudlak
Syndrome
Medical
Textbooks for Health Professionals and Consumers
► Hermansky-Pudlak Syndrome Network: Hermansky-Pudlak Syndrome Network Home Page ► International Albinism Center at the U. of Minnesota: International Albinism Center - Home Page ► Medical Object Oriented Softwere Enterprises: Hermanski-Pudlak Syndrome Diseases Database ► National Institute of Health /US/: Advances in Understanding the Hermansky-Pudlak Syndrome |
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© 2006, World
of Ophthalmology
Contact adress: v.zamyatin@gmail.com
