- Multiple familial trichoepithelioma
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Multiple familial trichoepithelioma (also known as "Brooke–Spiegler syndrome" and "Epithelioma adenoides cysticum") is a cutaneous condition characterized by multiple cystic and solid nodules appearing on the face.[1]:672
Types include:
Type OMIM Gene Locus MFT1 601606 CYLD 16q12-q13 MFT2 612099 ? 9p21 See also
- Trichofolliculoma
- Skin lesion
- List of cutaneous conditions
References
Hair Pilomatrixoma/Malignant pilomatricoma · Trichoepithelioma (Multiple familial trichoepithelioma, Solitary trichoepithelioma, Desmoplastic trichoepithelioma, Generalized trichoepithelioma) · Trichodiscoma · Trichoblastoma · Fibrofolliculoma · Trichilemmoma · Trichilemmal carcinoma · Giant solitary trichoepithelioma · Trichofolliculoma · Trichoadenoma
Hamartoma: Basaloid follicular hamartoma · Folliculosebaceous cystic hamartoma · Folliculosebaceous-apocrine hamartoma
Isthmicoma · Fibrofolliculoma · Perifollicular fibroma · Birt–Hogg–Dubé syndromeNails Translation Ribosome: Diamond–Blackfan anemia · FMR1 (Fragile X syndrome, Fragile X-associated tremor/ataxia syndrome, Premature ovarian failure 1)
Initiation factor: Leukoencephalopathy with vanishing white matter
snRNP: Retinitis pigmentosa 33Posttranslational modification E1: X-linked spinal muscular atrophy 2
E3: Johanson–Blizzard syndrome · Von Hippel–Lindau disease · 3-M syndrome · Angelman syndrome
Deubiquitinating enzyme: Machado–Joseph disease · Aneurysmal bone cyst · Multiple familial trichoepithelioma 1Othersee also genetic translation, posttranslational modification
B structural (perx, skel, cili, mito, nucl, sclr) · DNA/RNA/protein synthesis (drep, trfc, tscr, tltn) · membrane (icha, slcr, atpa, abct, othr) · transduction (iter, csrc, itra), trfkCategories:- Epidermal nevi, neoplasm, cyst stubs
- Epidermal nevi, neoplasms, cysts
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