Literatur
Beighton P (1970) Familial hypertrichosis cubiti: hairy elbows syndrome. J Med Genet 7(2):158–160
Polizzi A, Pavone P, Ciancio E, La Rosa C, Sorge G, Ruggieri M (2005) Hypertrichosis cubiti (hairy elbow syndrome): a clue to a malformation syndrome. J Pediatr Endocrinol Metab 18(10):1019–1025
Tng VE, de Zwaan S (2015) Hypertrichosis cubiti, a case report and literature review. Clin Case Rep 4(2):138–142. doi:10.1002/ccr3.465
Yuste-Chaves M, Zafra-Cobo MI, Martínez de Salinas A, Bravo-Piris J (2007) Two cases of hypertrichosis cubiti. Actas Dermosifiliogr 98(10):719–721
Andreev VC, Stransky L (1979) Hairy elbows. Arch Dermatol 115(6):761
Edwards MJ, Crawford AE, Jammu V, Wise G (1994) Hypertrichosis „cubiti“ with facial asymmetry. Am J Med Genet 53(1):56–58
MacDermot KD, Patton MA, Williams MJ, Winter RM (1989) Hypertrichosis cubiti (hairy elbows) and short stature: a recognisable association. J Med Genet 26(6):382–385
Flannery DB, Fink SM, Francis G, Gilman PA (1989) Hypertrichosis cubiti. Am J Med Genet 32(4):482–483
Warner TFCS, Hairy Elbows MD (1980) Hairy Elbows. Arch Dermatol 116(1):19
Rudolph RI (1985) Hairy elbows. Cutis 36(1):69. doi:10.1007/s00112-017-0245-9
Plantin P, Le Roux P, Larzul C, Le Noac’h E, Guillet G (1993) Hypertrichosis of the elbows. Ann Dermatol Venereol 120(10):701–703
Coleman R, Harper JI (1994) Hairy elbows syndrome (familial hypertrichosis cubiti). Clin Exp Dermatol 19(1):86–87
Miller ML, Yeager JK (1995) Hairy elbows. Arch Dermatol 131(7):858–859
Escalonilla P, Aguilar A, Gallego M, Piqué E, Fariña MC, Requena L (1996) A new case of hairy elbows syndrome (Hypertrichosis cubiti). Pediatr Dermatol 13(4):303–305
Di Lernia V, Neri I, Trevisi P, Patrizi A (1996) Hypertrichosis cubiti. Arch Dermatol 132(5):589
Lestringant GG, Frossard PM (1997) Hypertrichosis cubiti: A case in a Sri Lankan family. Int J Dermatol 36(3):235
Cambiaghi S, Pistritto G, Tadini G, Gelmetti C (1998) Hairy elbows. Int J Dermatol 37(4):317–318
Schwarze HP, Loche F, Kuchta J, Bazex J (1999) A sporadic form of hypertrichosis cubiti. Clin Exp Dermatol 24(6):497–498
Vashi RA, Mancini AJ, Paller AS (2001) Primary generalized and localized hypertrichosis in children. Arch Dermatol 137(7):877–884
Visser R, Beemer FA, Veenhoven RH, De Nef JJ (2002) Hypertrichosis cubiti: Two new cases and a review of the literature. Genet Couns 13(4):397–403
Rosina P, Pugliarello S, Tarocco M, D’Onghia FS, Barba A (2006) Hairy elbows syndrome. Int J Dermatol 45(2):127–128
Koç A, Karaer K, Ergün MA, Cinaz P, Perçin EF (2007) A new case of hairy elbows syndrome (hypertrichosis cubiti). Genet Couns 18(3):325–330
Nardello R, Mangano S, Fontana A, Tripi G, Didato MA, Di Pace M, Corsello G (2008) The hairy elbows syndrome: Clinical and neuroradiological findings. Pediatr Med Chir 30(5):262–264
León-Muiños E, Monteagudo B, Cabanillas M, Suárez-Amor O, Bermúdez E (2009) Hypertrichosis cubiti (hairy elbows syndrome). An Pediatr (Barc) 71(6):568–569. doi:10.1016/j.anpedi.2009.06.033
Martínez de Lagrán Z, González-Pérez R, Asunción Arregui-Murua M, Soloeta-Arechavala R (2010) Hypertrichosis cubiti: Another case of a well-recognized but under-reported entity. Pediatr Dermatol 27(3):310–311. doi:10.1111/j.1525-1470.2010.01148.x
Jones WD, Dafou D, McEntagart M, Woollard WJ, Elmslie FV, Holder-Espinasse M, Irving M, Saggar AK, Smithson S, Trembath RC, Deshpande C, Simpson MA (2012) De novo mutations in MLL cause Wiedemann-Steiner syndrome. Am J Hum Genet 91(2):358–364. doi:10.1016/j.ajhg.2012.06.008
Fernandez-Crehuet P, Ruiz-Villaverde R, Serrano JL (2013) Hairy elbows – A case study. Aust Fam Physician 42(11):801–802. doi:10.1007/s00112-017-0245-9
Dunkerton S, Field M, Cho V, Bertram E, Whittle B, Groves A, Goel H (2015) A de novo Mutation in KMT2A (MLL) in monozygotic twins with Wiedemann-Steiner syndrome. Am J Med Genet A 167A(9):2182–2187. doi:10.1002/ajmg.a.37130
Pavone V, Testa G, Falsaperla R, Sessa G (2015) A de novo Mutation in KMT2A (MLL) in monozygotic twins with Wiedemann-Steiner syndrome. Am J Med Genet A 167A(9):2182–2187. doi:10.1002/ajmg.a.37130
Steel D, Salpietro V, Phadke R, Pitt M, Gentile G, Massoud A, Batten L, Bashamboo A, Mcelreavey K, Saggar A, Kinali M (2015) Whole exome sequencing reveals a MLL de novo mutation associated with mild developmental delay and without ‚hairy elbows‘: expanding the phenotype of Wiedemann-Steiner syndrome. J Genet 94(4):755–758
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Kalampalikis, A., Tittelbach, J. & Elsner, P. Ungewöhnliche Behaarung einer jungen Patientin. Monatsschr Kinderheilkd 165, 373–376 (2017). https://doi.org/10.1007/s00112-017-0245-9
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DOI: https://doi.org/10.1007/s00112-017-0245-9