weber christian disease en
11Sturge-Weber syndrome — A congenital, but not inherited, disorder that affects the skin, the neurological system, and sometimes the eyes and internal organs. The main sign of Sturge Weber syndrome is a port wine stain birthmark. Neurological symptoms may include… …
12Rendu-Osler-Weber disease — Ren·du Os·ler Web·er disease .rän .d(y)ü äs lər web ər n HEREDITARY HEMORRHAGIC TELANGIECTASIA Ren·du rän due Henry Jules Louis Marie (1844 1902) French physician. Rendu was the leading French clinician of his day. His major writings include… …
13Christian-Weber disease — Chris·tian We·ber disease (krisґchən vaґbər) [H.A. Christian; Frederick Parkes Weber, English physician, 1863–1962] relapsing febrile nodular nonsuppurative panniculitis …
14Christian-Weber disease — relapsing febrile nodular nonsuppurative panniculitis …
15Huntington's disease — Classification and external resources A microscope image of …
16WCD — Weber Christian disease …
17WCD — • Weber Christian disease …
18panniculitis — Weber Christian disease; n. inflammation of the layer of fat beneath the skin, leading to multiple tender nodules in the legs and trunk …
19List of cutaneous conditions — This is an incomplete list, which may never be able to satisfy particular standards for completeness. You can help by expanding it with reliably sourced entries. See also: Cutaneous conditions, Category:Cutaneous conditions, and ICD 10… …
20panniculitis — Inflammation of subcutaneous adipose tissue. [panniculus + G. itis, inflammation] α1 antitrypsin deficiency p. multiple painful subcutaneous nodules occurring in patients with severe antitrypsin deficiency …
