- Scheie disease
- Scheie disease.См. мукополисахаридоз I.(Источник: «Англо-русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд-во ВНИРО, 1995 г.)
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Scheie disease — Scheie disease. = gargoilism (см.). (Источник: «Англо русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд во ВНИРО, 1995 г.) … Молекулярная биология и генетика. Толковый словарь.
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 — 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'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
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
connective tissue disease — Introduction any of the diseases that affect human connective tissue. Diseases of the connective tissue can be divided into (1) a group of relatively uncommon genetic disorders (genetic disease, human) that affect the primary structure of… … Universalium
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
мукополисахаридозы — mucopolysaccharidosis мукополисахаридозы. Группа НЗЧ, обусловленных дефектом ферментативного расщепления мукополисахаридов <mucopolysaccharides>; выделяют 7 типов М. синдром Гурлер, гаргоилизм <gargoylism>, болезни Санфилиппо… … Молекулярная биология и генетика. Толковый словарь.
мукополисахаридоз I — gargoilism, Hurler syndrome, Scheie disease гаргоилизм, синдром Гурлер, болезнь Шейе, мукополисахаридоз I. НЗЧ, обусловленное дефиицтом фермента α идуронидазы и проявляющееся в своеобразных чертах лица (голова увеличена по типу долихоцефалии),… … Молекулярная биология и генетика. Толковый словарь.
Mucopolysaccharidosis — MPS I redirects here. For zhuyin or bopomofo, a phonetic system for romanizing Chinese, also known as Mandarin Phonetic Symbols I, see Bopomofo. Mucopolysaccharidosis Classification and external resources ICD 10 E76 ICD 9 … Wikipedia