I-cell disease: clinical studies of 21 Japanese cases

التفاصيل البيبلوغرافية
العنوان: I-cell disease: clinical studies of 21 Japanese cases
المؤلفون: Tohru Yutaka, Minoru Ogawa, Takeshi Sakiyama, Shintaro Okada, Misao Owada
المصدر: Clinical genetics. 28(3)
سنة النشر: 1985
مصطلحات موضوعية: Male, medicine.medical_specialty, Pediatrics, Adolescent, Cardiovascular Abnormalities, Cardiomyopathy, Transferases (Other Substituted Phosphate Groups), Cardiomegaly, Disease, Sudden death, Bone and Bones, Mucolipidoses, Internal medicine, Genetics, medicine, Humans, Child, Respiratory Tract Infections, Genetics (clinical), Motor skill, Growth Disorders, Psychomotor retardation, Coarse facial features, business.industry, Phosphotransferases, Hypertrophic cardiomyopathy, Infant, medicine.disease, Endocrinology, Child, Preschool, Female, I-cell disease, medicine.symptom, Psychomotor Disorders, business
الوصف: Clinical pictures of 21 cases with I-cell disease patients, 12 males and 9 females, were analyzed. Characteristic coarse facial features and shortness of stature were observed in all cases. In general, the motor development was found to be more severely retarded than the mental development of the patients. Rather little involvement of the nervous system seemed to cause somewhat acceptable mental development in some cases, and also cause the absence of epileptic seizures in all cases. Involvement of the cardiovascular system, especially progressive hypertrophic cardiomyopathy, could be highly responsible for frequent sudden death of I-cell disease patients.
تدمد: 0009-9163
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::948be412ce39130049f80968083b51ccTest
https://pubmed.ncbi.nlm.nih.gov/2998652Test
حقوق: CLOSED
رقم الانضمام: edsair.doi.dedup.....948be412ce39130049f80968083b51cc
قاعدة البيانات: OpenAIRE