| Recklinghausen's disease of bone | Rarefying osteitis with fibrous degeneration and formation of cysts, and with the presence of fibrous nodules on the affected bones. It is due to marked osteoclastic activity secondary to hyperfunction of the parathyroid glands. (12 Dec 1998) |
|---|---|
| Recklinghausen's disease type I | type 2 neurofibromatosis |
| central Recklinghausen's disease type II | type 1 neurofibromatosis |
| von Recklinghausen disease | type 1 neurofibromatosis |
| von Recklinghausen's disease | <disease> A rare genetic disorder which affects the cell growth of nerve tissue. Individuals have multiple cutaneous and subcutaneous tumours which appear in late childhood. Clinical features include medium-brown, flat discolourations to the skin, known as cafe-au-lait spots. Secondary hypertension may develop from renal artery stenosis, pheochromocytoma or coarctation of the aorta. Inheritance: autosomal dominant. (04 Nov 1997) |
| disease, von recklinghausen's | Hereditary disorder characterised by cafe-au-lait (coffee-with-milk spots on the skin and a tendency to develop nerve tumours) also known as neurofibromatosis. (12 Dec 1998) |
| Recklinghausen | Friedrich D. Von, German histologist and pathologist, 1833-1910. See: central Recklinghausen's disease type II, Recklinghausen's disease of bone, Recklinghausen's disease type I, Recklinghausen's tumour, von Recklinghausen disease. (05 Mar 2000) |
| Recklinghausen's tumour | A small, circumscribed, benign tumour of the genital tract, composed of small glandlike spaces lined by flattened or cuboidal mesothelium-like cells. (12 Dec 1998) |
| bone within a bone | <radiology> STOP heavy metal, S: sickle cell disease, T: Thorotrast, O: osteopetrosis, P: Paget's disease, heavy metals, hypervitaminosis D (12 Dec 1998) |
| marble bone disease | The formation of abnormally dense bone, as opposed to osteoporosis. (18 Nov 1997) |
| gorham's vanishing bone disease | <radiology> Massive osteolysis of Gorham, painless, occurs in kids and young adults, not life-threatening unless vital structures are encroached upon, some recover spontaneously, with or without residual deformity, complete destruction of part or all of bone by angiomatous tissue, usually unifocal, affects proximal skeleton, may spread into soft tissues and adjacent bones Cf: other syndromes of spontaneous osteolysis (12 Dec 1998) |
| disappearing bone disease | Extensive decalcification of a single bone; of unknown cause, sometimes associated with angioma. Synonym: Gorham's disease. (05 Mar 2000) |
| acute reflex bone atrophy | Atrophy of bones, commonly of the carpal or tarsal bones, following a slight injury such as a sprain. See: causalgia, reflex sympathetic dystrophy. Synonym: acute reflex bone atrophy, posttraumatic osteoporosis, Sudeck's syndrome. Origin: L. English sweat (05 Mar 2000) |
| air-bone gap | The difference between the threshold for hearing acuity by bone conduction and by air conduction. (05 Mar 2000) |
| Albrecht's bone | A small bone between the basioccipital and basisphenoid. (05 Mar 2000) |