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1 болезнь Шейе
1) Medicine: Hurler disease, lipochondrodystrophy, Pfaundler-Hurler syndrome, type IH mucopolysaccharidosis, mucopolysaccharidosis type I, alpha-L-iduronidase deficiency, Hurler-Scheie syndrome, IDUA deficiency, mucopolysaccharidosis I, Scheie syndrome, Pfaundler-Hurler disease, Hurler's disease2) Genetics: Hurler syndrome, Scheie disease, gargoilism -
2 мукополисахаридоз I типа
Универсальный русско-английский словарь > мукополисахаридоз I типа
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3 болезнь Пфаундлера-Гурлера
Medicine: lipochondrodystrophy, Pfaundler-Hurler syndrome, type IH mucopolysaccharidosis, mucopolysaccharidosis type I, alpha-L-iduronidase deficiency, Hurler-Scheie syndrome, IDUA deficiency, mucopolysaccharidosis I, Scheie syndrome, Pfaundler-Hurler disease, Hurler's disease, Hurler disease, Hurler syndromeУниверсальный русско-английский словарь > болезнь Пфаундлера-Гурлера
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4 болезнь Пфаундлера-Гурлера-Эллиса
Medicine: lipochondrodystrophy, Pfaundler-Hurler syndrome, type IH mucopolysaccharidosis, mucopolysaccharidosis type I, alpha-L-iduronidase deficiency, Hurler-Scheie syndrome, IDUA deficiency, mucopolysaccharidosis I, Scheie syndrome, Pfaundler-Hurler disease, Hurler's disease, Hurler disease, Hurler syndromeУниверсальный русско-английский словарь > болезнь Пфаундлера-Гурлера-Эллиса
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5 полидистрофия Гурлера-Эллиса
Medicine: lipochondrodystrophy, Pfaundler-Hurler syndrome, type IH mucopolysaccharidosis, mucopolysaccharidosis type I, alpha-L-iduronidase deficiency, Hurler-Scheie syndrome, IDUA deficiency, mucopolysaccharidosis I, Scheie syndrome, Pfaundler-Hurler disease, Hurler's disease, Hurler syndrome, Hurler diseaseУниверсальный русско-английский словарь > полидистрофия Гурлера-Эллиса
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6 болезнь Гурлера
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7 мукополисахаридоз I
Универсальный русско-английский словарь > мукополисахаридоз I
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8 синдром Шейе
Scheie's syndrome, type V mucopolysaccharidosisБольшой русско-английский медицинский словарь > синдром Шейе
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9 E76.0
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10 гаргоилизм
1) General subject: Brailsford-Morquio disease (мукополисахаридоз 1 и 2 типов, заболевание, обусловленное наследственной патологией соединительной ткани, проявляющееся поражением костей, суставов, глаз, внутренних органов и нерв)2) Medicine: Hunter's syndrome, Hurler's syndrome, dysostosis multiplex, gargoylism3) Genetics: Hurler syndrome, Scheie disease, gargoilism -
11 синдром Гурлер
1) Medicine: Hurler's syndrome (болезнь)2) Genetics: Hurler syndrome, Scheie disease, gargoilism -
12 мукополисахаридоз V типа
type V mucopolysaccharidosis, Scheie's syndromeБольшой русско-английский медицинский словарь > мукополисахаридоз V типа
См. также в других словарях:
Scheie syndrome — shī n an autosomal recessive mucopolysaccharidosis similar to Hurler s syndrome but less severe that is characterized by clouding of the cornea, slight deformity of the extremities, and disease of the aorta but not by mental retardation or early… … Medical dictionary
Scheie syndrome — (also known as MPS V) ) is less severe version of Hurler s disease. It is a condition characterized by corneal clouding, facial dysmorphism, and normal lifespan [1] but unlike Hurler s, disease has normal intellect and .[2] See also Sanfilippo… … Wikipedia
Scheie syndrome — Mucopolysaccharidosis (lysosomal disease) in which there is a defect in a L iduronidase. Fibroblasts from Scheie syndrome patients do not cross correct fibroblasts from Hurler&’s disease, although the two conditions are clinically distinct … Dictionary of molecular biology
Hurler–Scheie syndrome — (also known as Mucopolysaccharidosis type I H S ) is a cutaneous condition, also characterized by mild mental retardation and corneal clouding.[1] See also Scheie syndrome List of cutaneous conditions References ^ Rapini, Ronald P.; Bolognia,… … Wikipedia
Hurler-Scheie syndrome — Hur·ler Scheie syndrome (hurґlər shaґ) [G. Hurler; Harold G. Scheie, American ophthalmologist, 1909–1990] see under syndrome … Medical dictionary
Hurler-Scheie syndrome — Although clinically distinct diseases, fibroblasts from patients with Hurler s and with Scheie syndrome do not cross complement in culture, suggesting that the enzyme defect is the same … Dictionary of molecular biology
Hurler-Scheie syndrome — one of the three allelic disorders of mucopolysaccharidosis I, with clinical features intermediate between the Hurler and the Scheie syndromes, caused by deficiency of L iduronidase, and specifically characterized by receding chin (micrognathism) … Medical dictionary
Syndrome, Hurler — An inherited error of metabolism in which there is deficiency of the enzyme alpha L iduronidase which normally breaks down molecules called mucopolysaccharides. Without the activity of this enzyme, there is an abnormal accumulation of… … Medical dictionary
Scheie's syndrome — ▪ pathology also called Mucopolysaccharidosis I S , or Mps I S uncommon hereditary metabolic disease characterized by clawing of the hands, corneal clouding, incompetence of the aortic valve of the heart, and painful nerve compression in … Universalium
Syndrome de Hurler-Scheie-Hurler/Scheie — Syndrome de Hurler Syndrome de Hurler Autre nom Mucopolysaccharidose de type 1 Référence MIM … Wikipédia en Français
syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… … Medical dictionary