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11 Possible Causes for Hoffa's, Disease, liposynovitis, or, prepatellaris

  • Farber Disease

    272.8 Disease, diseased - see also Syndrome Anders' (adiposis tuberosa simplex) 272.8 Dercum's (adiposis dolorosa) 272.8 Farber's (disseminated lipogranulomatosis) 272.8 Hoffa[icd9data.com] American Journal of Diseases of Children, Chicago, 1952, 84: 499-500. S. Farber, J. Cohen, L. L. Uzman: Lipogranulomatosis: A new lipo-glyco-protein “storage” disease.[whonamedit.com] Genetic counseling Farber disease is inherited in an autosomal recessive manner. Genetic counseling is possible.[orpha.net] […] prepatellaris Madelung's neck Nodular circumscribed lipomatosis Nodular fat necrosis Oil granuloma Phytanic acid storage disease Proteinosis Traumatic fat necrosis Applies To Hoffa's[icd9data.com] Author information 1 Pediatrics Department, Hassan II University Hospital, Fez, Morocco. [email protected] Abstract Farber disease is a rare lysosomal storage disease[ncbi.nlm.nih.gov]

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  • Adiposis Dolorosa

    272.8 Disease, diseased - see also Syndrome Anders' (adiposis tuberosa simplex) 272.8 Dercum's (adiposis dolorosa) 272.8 Farber's (disseminated lipogranulomatosis) 272.8 Hoffa[icd9data.com] […] for lipomas seen in patients with Dercum’s disease in adulthood.”[dercumsdiseaseresearch.wordpress.com] Dercum disease questionnaire If you or any one you know suffers from this disease, please fill out the questionnaire![dercum.org] A weight shape index for assessing risk of disease in 44,820 women . J Clin Epidemiol 1988; 41 : 459–465. 30. Te C , Herbst KL.[dx.doi.org] A large number of patients develop malignant tumors (carcinomas, sarcomas, and lymphomas) Applies To Hoffa's disease or liposynovitis prepatellaris Launois-Bensaude's lipomatosis[icd9data.com]

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  • Erdheim-Chester Disease

    […] disease E88.89 Hoffa's disease E88.89 Ketosis NEC E88.89 Launois-Bensaude adenolipomatosis E88.89 Lipomatosis E88.2 ICD-10-CM Diagnosis Code E88.2 Lipomatosis, not elsewhere[icd10data.com] Erdheim–Chester disease (also known as Erdheim–Chester syndrome or polyostotic sclerosing histiocytosis) is a rare disease characterized by the abnormal multiplication of[en.wikipedia.org] After a careful observation for the disease progression, he underwent bilateral deceased-donor lung transplantation.[ncbi.nlm.nih.gov] Abstract Erdheim-Chester disease (ECD) is a rare, non-Langerhans cell histiocytosis with classic radiographic findings of patchy or diffuse osteosclerosis predominantly involving[ncbi.nlm.nih.gov] […] elsewhere classified 2016 2017 2018 2019 Billable/Specific Code Applicable To Lipomatosis NOS Lipomatosis (Check) dolorosa [Dercum] Launois-Bensaude E88.89 Liposynovitis prepatellaris[icd10data.com]

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  • Multiple Symmetric Lipomatosis

    272.8 Disease, diseased - see also Syndrome Anders' (adiposis tuberosa simplex) 272.8 Dercum's (adiposis dolorosa) 272.8 Farber's (disseminated lipogranulomatosis) 272.8 Hoffa[icd9data.com] Abstract Multiple symmetric lipomatosis (Madelung's disease) is a rare disease characterized by non-encapsulated adipose deposits in the neck, the superior part of the trunk[ncbi.nlm.nih.gov] Familiarity has been reported and MSL is considered an autosomic dominant inherited disease.[ncbi.nlm.nih.gov] The recognition of this disease is important as, in addition to cosmetic abnormality, it can compress the important neurovascular structures.[ncbi.nlm.nih.gov] A large number of patients develop malignant tumors (carcinomas, sarcomas, and lymphomas) Applies To Hoffa's disease or liposynovitis prepatellaris Launois-Bensaude's lipomatosis[icd9data.com]

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  • Lipoid Proteinosis

    272.8 Disease, diseased - see also Syndrome Anders' (adiposis tuberosa simplex) 272.8 Dercum's (adiposis dolorosa) 272.8 Farber's (disseminated lipogranulomatosis) 272.8 Hoffa[icd9data.com] […] can be carriers of the disease but show no symptoms.[en.wikipedia.org] - A dictionary of medical eponyms Related people Camillo Wiethe Erich Urbach Robert Rössle A very rare, congenital lipoid storage disease with multiple lipoid infiltrations[whonamedit.com] Cinaz P, Guvenir T, Gonlusen G: Lipoid proteinosis: Urbach-Wiethe disease. Acta Paediatr 1993;82:892–893.[dx.doi.org] A large number of patients develop malignant tumors (carcinomas, sarcomas, and lymphomas) Applies To Hoffa's disease or liposynovitis prepatellaris Launois-Bensaude's lipomatosis[icd9data.com]

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  • Rothmann-Makai Syndrome

    272.8 Disease, diseased - see also Syndrome Anders' (adiposis tuberosa simplex) 272.8 Dercum's (adiposis dolorosa) 272.8 Farber's (disseminated lipogranulomatosis) 272.8 Hoffa[icd9data.com] Clinical Reference / Quandaries in Dermatology / Weber-Christian Syndrome, Rothmann-Makai Disease, Sulzberger-Garbe Disease, Miescher’s Granuloma Disciformis, and Unna’s Hard[derm101.com] Today, the more frequent associations include streptococcal infections, sarcoidosis, ulcerative colitis and Crohn’s disease, Sweet’s syndrome, Behçet’s disease, menstruation[basicmedicalkey.com] […] prepatellaris Madelung's neck Nodular circumscribed lipomatosis Nodular fat necrosis Oil granuloma Phytanic acid storage disease Proteinosis Traumatic fat necrosis Applies To Hoffa's[icd9data.com] […] of collagen diseases.[docslide.us]

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  • Launois Syndrome

    […] disease E88.89 Hoffa's disease E88.89 Ketosis NEC E88.89 Launois-Bensaude adenolipomatosis E88.89 Lipomatosis E88.2 ICD-10-CM Diagnosis Code E88.2 Lipomatosis, not elsewhere[icd10data.com] Abstract A case of Launois-Bensaude Syndrome (Madelung's disease) in a chronic alcoholic is presented and the typical features are discussed.[ncbi.nlm.nih.gov] METHODS: The current treatment of the disease is described based on the authors' experience.[ncbi.nlm.nih.gov] Methods The current treatment of the disease is described based on the authors’ experience.[link.springer.com] […] elsewhere classified 2016 2017 2018 2019 Billable/Specific Code Applicable To Lipomatosis NOS Lipomatosis (Check) dolorosa [Dercum] Launois-Bensaude E88.89 Liposynovitis prepatellaris[icd10data.com]

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  • Leri's Pleonosteosis Syndrome

    […] tenosynovitis Dupuytren’s contracture Farber’s disease Felty’s syndrome Francoise syndrome Gaucher’s disease Handigodu syndrome Heberden’s nodes Henoch-Schönlein purpura Hoffa’s[the-rheumatologist.org] Neoplasm, connective tissue, malignant Lipoprotein metabolism disorder E78.9 Lipoproteinemia E78.5 Liposarcoma - see also Neoplasm, connective tissue, malignant Liposynovitis prepatellaris[icd.codes] Key points Comprehensive guide to ocular syndromes and systemic diseases Presents alphabetically, more than 1600 common and uncommon disorders and diseases Written by internationally[books.google.com] 103 OSTEOCHONDRITIS DISSECANS 104 OSTEOCHONDROMATOSIS 105 OSTEOMALACIA and RICKETS 106 PALINDROMA RHEUMATISM 107 PANCREATIC CARCINOMA and ACUTE PANCREATITIS 108 PERTHES DISEASE[books.google.es] A list of disease s in the English wikipedia.[en.academic.ru]

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  • Prepatellar Bursitis

    […] of the distal prepatellar bursa with prepatellar thickened bursa Deep infrapatellar bursa: Bursitis of the deep infrapatellar bursa with fluid filled bursa and echogenic Hoffa[ultrasoundcases.info] , bursitis; prepatellair , hygroom; prepatellair , prepatellair; bursitis , prepatellair; hygroom , Bursitis prepatellaris French Bursite prérotulienne , Bursite pré-rotulienne[fpnotebook.com] […] for Joint Diseases, New York, New York.[ncbi.nlm.nih.gov] Prepatellar bursitis is an inflammatory process at the anterior part of the knee, ie. an inflammation of the prepatellar bursa ( bursa prepatellaris ), a soft, filled with[videoreha.com] The case illustrates the importance of repeatedly aspirating suspicious sites to establish the diagnosis in elusive cases of crystal deposition disease.[ncbi.nlm.nih.gov]

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  • Cytosolic Acetoacetyl-CoA Thiolase Deficiency

    […] deficiency Intestinal obstruction in newborn due to guanylate cyclase 2C deficiency Ketonemia Ketosis Ketotic hypoglycemia Laminopathy type Decaudain Vigouroux Liposynovitis prepatellaris[icdlist.com] Brief reference to other diagnostic possibilities is also given in all disease-related chapters.[books.google.com] This now includes a chapter on the clinical presentation of metabolic diseases in the older age range, using an analogous structure.[books.google.com] The authors are acknowledged experts, and the book will be a valuable desk reference for all who deal with inherited metabolic diseases.[books.google.com] […] enteropeptidase deficiency Intestinal obstruction in newborn due to guanylate cyclase 2C deficiency Ketonemia Ketosis Ketotic hypoglycemia Laminopathy type Decaudain Vigouroux Liposynovitis[icdlist.com]

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