Prader-Willi syndrome with Oculocutaneous Albinism: Anaesthetic Implications and Management
Prader-Willi syndrome is a rare congenital disorder characterized by obesity, hypotonia, hypogonadism and developmental delay. The genetic disorder is caused by microdeletion on chromosome 15 on the paternal chromosome. The syndrome is a 2-stage disorder with hypotonic early infantile phase and...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
JCDR Research and Publications Pvt. Ltd.
2014-04-01
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| Series: | National Journal of Laboratory Medicine |
| Subjects: | |
| Online Access: | http://www.njlm.net/articles/PDF/2007/4-%206780_F(H)_PF1(PAG)_PFA(AK)_PF2(AGAK).pdf |