Osteopetro-rickets : a new cogenital bone disorder

التفاصيل البيبلوغرافية
العنوان: Osteopetro-rickets : a new cogenital bone disorder
المؤلفون: D. Buffe, Milhaud G, Y. Moricard, Labat Ml, M. Juster, Moutier R, C. Rimbaut, I. Litwin
المصدر: Metabolic Bone Disease and Related Research. 3:91-97
بيانات النشر: Elsevier BV, 1981.
سنة النشر: 1981
مصطلحات موضوعية: Calcitonin, medicine.medical_specialty, Bone disease, Developmental defect, Endocrinology, Diabetes and Metabolism, Mutant, Rickets, Thymus Gland, Bone and Bones, Rats, Mutant Strains, Internal medicine, Animals, Medicine, Thymic atrophy, business.industry, Osteoid, Body Weight, Phosphorus, Osteopetrosis, Alkaline Phosphatase, medicine.disease, Rats, Disease Models, Animal, Phenotype, Endocrinology, Bone lesion, Surgery, alpha-Fetoproteins, business
الوصف: Two lethal nwtations have been described in the rat: ⪡ osteopetrosis ⪢ (op) and , ⪡ toothless ⪢ (tl). The op mutant can be cured by normal bone marrow infusion, while the tl mutant cannot. We report here additional data with regard to the tl mutant. The bone disease of the tl rat as in the op rat Is associated with a ,precocious thymic atrophy, but bone lesions are quite different. In addition to classical osteopetrosis, the tl rat displays several features of rickets: broadening of the extremities of long bones, thickening of the epiphyseal plates, presence of osteoid areas. In addition, the persistence of embryonic characters, evidenced by high levels of alpha-fetoprotein, suggests that the developmental defect of bone is part of a more general process.
تدمد: 0221-8747
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06bef01addf22ba448aee4eac6257bf1
https://doi.org/10.1016/0221-8747(81)90026-6
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....06bef01addf22ba448aee4eac6257bf1
قاعدة البيانات: OpenAIRE