Hermansky-Pudlak disease

Hermansky-Pudlak disease
Медицина: синдром Германского-Пудлака (наследственный тирозин-негативный альбинизм в сочетании с дефектом тромбоцитов и геморрагическим диатезом), болезнь Хержманского-Пудлака

Универсальный англо-русский словарь. . 2011.

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Смотреть что такое "Hermansky-Pudlak disease" в других словарях:

  • Hermansky–Pudlak syndrome — Classification and external resources ICD 10 E70.3 (ILDS E70.360) OMIM 203300 …   Wikipedia

  • Hermansky-Pudlak syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 29161 ICD10 = ICD10|E|70|3|e|70 (ILDS E70.360) ICD9 = ICDO = OMIM = 203300 MedlinePlus = eMedicineSubj = oph eMedicineTopic = 713 eMedicine mult = eMedicine2|derm|925 | MeshID = D022861… …   Wikipedia

  • Hermansky-Pudlak syndrome (HPS) — A genetic disorder characterized by albinism (with lack of pigment in the skin or eye), bruising and prolonged bleeding (due to defective blood platelets), and fibrosis of the lungs. There is occasionally also inflammatory bowel disease and… …   Medical dictionary

  • HPS (Hermansky-Pudlak syndrome) — A genetic (inherited) disorder characterized by albinism (with lack of skin and eye pigment), bruising and prolonged bleeding (due to defective blood platelets), and fibrosis of the lungs. In HPS there is occasionally also inflammatory bowel… …   Medical dictionary

  • Syndrome, Hermansky-Pudlak (HPS) — A genetic (inherited) disorder characterized by albinism (with lack of skin and eye pigment), bruising and prolonged bleeding (due to defective blood platelets), and fibrosis of the lungs. In HPS there is occasionally also inflammatory bowel… …   Medical dictionary

  • Disease, delta-storage pool — A genetic (inherited) disorder, also known as the Hermansky Pudlak syndrome (HPS), characterized by albinism (with lack of skin and eye pigment), bruising and prolonged bleeding (due to defective blood platelets), and fibrosis of the lungs. In… …   Medical dictionary

  • Charcot–Marie–Tooth disease — Charcot Marie Tooth disease Classification and external resources The foot of a person with Charcot Marie Tooth. The lack of muscle, a high arch, and claw toes are signs of the genetic disease. ICD 10 …   Wikipedia

  • Delta-storage pool disease — A genetic (inherited) disorder, also known as the Hermansky Pudlak syndrome (HPS), characterized by albinism (with lack of skin and eye pigment), bruising and prolonged bleeding (due to defective blood platelets), and fibrosis of the lungs. In… …   Medical dictionary

  • Sickle-cell disease — This article is about the disease itself. For the genetic transmission of sickle cell disease and its carrier state, see sickle cell trait. Sickle cell disease Classification and external resources Normal and sickle shaped red blood cells ICD 10 …   Wikipedia

  • Maple syrup urine disease — Classification and external resources Isoleucine (pictured above), leucine, and valine are the branched chain amino acids that build up in MSUD. ICD …   Wikipedia

  • Cold agglutinin disease — Classification and external resources Cold agglutination at body temperature, the antibodies do not attach to the red blood cells. At lower temperatures, however, the antibodies react to Ii antigens, bringing the red blood cells together, a… …   Wikipedia


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