Hermanski-Pudlaka's band


Hermansky-Pudlab syndrome (HPS), a rare, genetically-conditioned syndrome, clinically manifested as an increase in bleeding time and ocular albinism. Inheritance of the disease is autosomal recessive. Platelets lack δ. The disease was described by Czech interlocutors František Heřmanský and Pavel Pudlák in 1959. At least eight gene loci have been identified, whose mutations appear clinically as a syndrome of Heřmansky and Pudlák.

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