| McLean t. |
impression t.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| McLeod p. |
a rare blood phenotype with X-linked inheritance in which several antigens of the Kell blood group are weakly expressed; affected individuals sometimes have an anemic condition called McLeod syndrome.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| McLeod phenotype, syndrome |
see under phenotype and syndrome.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| McLeod s. |
a syndrome seen in some individuals having the McLeod phenotype of blood, characterized by mild hemolytic anemia with acanthocytes, elevated serum creatinine phosphokinase, and sometimes muscle wasting and neurological defects. A few cases have manifested as X-linked types of chronic granulomatous disease.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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