BIOMAT Database Logo BIOMAT Database Logo

[Weber-Christian syndrome associated with an alpha-1 antitrypsin deficiency. Familial investigation]. 1972

J Warter, and D Storck, and E Grosshans, and P Metais, and J L Kuntz, and T Klumpp

UI MeSH Term Description Entries
D007592 Joint Diseases Diseases involving the JOINTS. Arthropathies,Arthropathy,Joint Disease
D008661 Metabolism, Inborn Errors Errors in metabolic processes resulting from inborn genetic mutations that are inherited or acquired in utero. Inborn Errors of Metabolism,Metabolism Errors, Inborn,Error, Inborn Metabolism,Errors Metabolism, Inborn,Errors Metabolisms, Inborn,Errors, Inborn Metabolism,Inborn Errors Metabolism,Inborn Errors Metabolisms,Inborn Metabolism Error,Inborn Metabolism Errors,Metabolism Error, Inborn,Metabolism Inborn Error,Metabolism Inborn Errors,Metabolisms, Inborn Errors
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D010146 Pain An unpleasant sensation induced by noxious stimuli which are detected by NERVE ENDINGS of NOCICEPTIVE NEURONS. Suffering, Physical,Ache,Pain, Burning,Pain, Crushing,Pain, Migratory,Pain, Radiating,Pain, Splitting,Aches,Burning Pain,Burning Pains,Crushing Pain,Crushing Pains,Migratory Pain,Migratory Pains,Pains, Burning,Pains, Crushing,Pains, Migratory,Pains, Radiating,Pains, Splitting,Physical Suffering,Physical Sufferings,Radiating Pain,Radiating Pains,Splitting Pain,Splitting Pains,Sufferings, Physical
D010201 Panniculitis, Nodular Nonsuppurative A form of panniculitis characterized by recurrent episodes of fever accompanied by the eruption of single or multiple erythematous subcutaneous nodules on the lower extremities. They normally resolve, but tend to leave depressions in the skin. The condition is most often seen in women, alone or in association with other disorders. Weber-Christian Disease,Disease, Weber-Christian,Nodular Nonsuppurative Panniculitides,Nodular Nonsuppurative Panniculitis,Nonsuppurative Panniculitides, Nodular,Nonsuppurative Panniculitis, Nodular,Panniculitides, Nodular Nonsuppurative,Weber Christian Disease
D010375 Pedigree The record of descent or ancestry, particularly of a particular condition or trait, indicating individual family members, their relationships, and their status with respect to the trait or condition. Family Tree,Genealogical Tree,Genealogic Tree,Genetic Identity,Identity, Genetic,Family Trees,Genealogic Trees,Genealogical Trees,Genetic Identities,Identities, Genetic,Tree, Family,Tree, Genealogic,Tree, Genealogical,Trees, Family,Trees, Genealogic,Trees, Genealogical
D012008 Recurrence The return of a sign, symptom, or disease after a remission. Recrudescence,Relapse,Recrudescences,Recurrences,Relapses
D005260 Female Females
D005334 Fever An abnormal elevation of body temperature, usually as a result of a pathologic process. Pyrexia,Fevers,Pyrexias
D006406 Hematoma A collection of blood outside the BLOOD VESSELS. Hematoma can be localized in an organ, space, or tissue. Hematomas

Related Publications

J Warter, and D Storck, and E Grosshans, and P Metais, and J L Kuntz, and T Klumpp
[Weber-Christian disease associated with familial alpha-1-antitrypsin deficiency. Apropos of a case].
January 1985, Annales de dermatologie et de venereologie,
J Warter, and D Storck, and E Grosshans, and P Metais, and J L Kuntz, and T Klumpp
Familial occurrence of alpha 1-antitrypsin deficiency and Weber-Christian disease.
March 1983, Archives of dermatology,
J Warter, and D Storck, and E Grosshans, and P Metais, and J L Kuntz, and T Klumpp
[Alpha-1-antitrypsin deficiency in Weber-Christian panniculitis].
January 1981, Actas dermo-sifiliograficas,
J Warter, and D Storck, and E Grosshans, and P Metais, and J L Kuntz, and T Klumpp
Cyclophosphamide therapy for Weber-Christian disease associated with alpha 1-antitrypsin deficiency.
November 1986, Southern medical journal,
J Warter, and D Storck, and E Grosshans, and P Metais, and J L Kuntz, and T Klumpp
Familial hypercholesterolaemia with alpha 1-antitrypsin deficiency.
February 1978, British medical journal,
J Warter, and D Storck, and E Grosshans, and P Metais, and J L Kuntz, and T Klumpp
Genetic study of a family with two members with Weber Christian disease (panniculitis) and alpha 1 antitrypsin deficiency.
September 1982, American journal of medical genetics,
J Warter, and D Storck, and E Grosshans, and P Metais, and J L Kuntz, and T Klumpp
[Familial deficiency on alpha-1-antitrypsin].
January 1971, Zeitschrift fur Kinderheilkunde,
J Warter, and D Storck, and E Grosshans, and P Metais, and J L Kuntz, and T Klumpp
Familial emphysema and alpha 1-antitrypsin deficiency.
January 1967, Aspen Emphysema Conference,
J Warter, and D Storck, and E Grosshans, and P Metais, and J L Kuntz, and T Klumpp
Familial emphysema and alpha-1-antitrypsin deficiency.
December 1966, The New England journal of medicine,
J Warter, and D Storck, and E Grosshans, and P Metais, and J L Kuntz, and T Klumpp
Familial hypogammaglobulinemia. Genetic linkage with alpha 1-antitrypsin deficiency.
March 1983, Archives of internal medicine,
Copied contents to your clipboard!