intermediate filament disorder
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Etiology
Keratin-related disorders
- chronic pancreatitis
- hepatic cirrhosis & hepatitis
- epidermolysis bullosa simplex
- epidermolytic hyperkeratosis
- ichthyosis bullosa of Siemens
- inflammatory bowel disease
- loose anagen syndrome
- Meesmann corneal dystrophy
- monilethrix
- oral white-sponge nevus
- pachyonychia congenita
- palmoplantar keratoderma
- epidermolytic
- nonepidermolytic
- striate
- pseudofollicultis barbae
- steatocystoma multiplex
Lamin-related disorders
- atrial fibrillation, early onset
- Charcot-Marie-Tooth disease, type 2B1
- dilated cardiomyopathy, type 1A
- familial partial lipodystrophy
- Hutchinson-Gilford progeria
- lipoatrophy with diabetes, hepatic steatosis, hypertrophic cardiomyopathy & leukomelanodermic papules (LDHCP)
- mandibuloacral dysplasia
- muscular dystrophy
- Werner's syndrome, atypical
Other
- Alexander disease
- amyotrophic lateral sclerosis, sporadic form
- cataracts, juvenile onset
- Charcot-Marie-Tooth disease, types 1F & 2E
- dilated cardiomyopathy, type 2
- desmin-related myopathy
More general terms
More specific terms
Additional terms
References
- ↑ Omary MB, Coulombe PA, McLean WH. Intermediate filament proteins and their associated diseases. N Engl J Med. 2004 Nov 11;351(20):2087-100. Review. PMID: https://www.ncbi.nlm.nih.gov/pubmed/15537907