Long-Arm Deletion of Chromosome 22, with Protein-Losing Enteropathy
نویسندگان
چکیده
منابع مشابه
[Protein-losing enteropathy].
Protein-losing enteropathy (PLE) is a rare complication of intestinal diseases. Its main manifestation is hypoproteinemic edema. The diagnosis of PLE is based on the verification of protein loss into the intestinal lumen, by determining fecal α1-antitrypsin concentration and clearance. The localization of the affected colonic segment is clarified using radiologic and endoscopic techniques. The ...
متن کاملCap polyposis with protein-losing enteropathy.
A 56-year-old male with a history of mild mental retardation, noninsulin-dependent diabetes mellitus, and hypertension presented with diarrhea and lower extremity edema of several months’ duration. The patient’s symptoms started with mild, intermittent diarrhea; several months later, his diarrhea became persistent, and he was admitted to a hospital. The patient was given metronidazole (Flagyl, ...
متن کاملProtein losing enteropathy associated with collagen diseases.
Four patients with collagen diseases are described, who developed protein losing enteropathy in the course of their disease. Their protein losing enteropathies subsided after treatment with 60 mg/day oral prednisolone. Immunohistological studies of the small intestine showed deposits of C3 in the capillary walls of villi in two patients. Increased capillary permeability due to autoimmune phenom...
متن کاملProtein losing enteropathy in children
Sum mary Protein-losing enteropathy is a medical condition which is characterized by loss of protein, vitamin and trace elements into the intestines which can be complicated by various diseases. The main causes of protein-losing enteropathy in children are primary or secondary intestinal lymphangiectesia, Menetrier disease, inflammatory and immunological disorders. Hypoalbuminemia, developed du...
متن کاملDeletion mapping of the long arm of chromosome 22 in human meningiomas.
Cytogenetic and molecular genetic analyses have shown that a tumor-suppressor gene for human meningioma is located on the long arm of chromosome 22. Recently, somatic mutations of the NF2 gene have been identified in sporadic meningiomas. However, tumorigenesis of certain cases of meningioma cannot be fully explained by inactivation of the NF2 gene alone. Thus, to obtain some indication as to t...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Proceedings of the Royal Society of Medicine
سال: 1972
ISSN: 0035-9157
DOI: 10.1177/003591577206501212