View Item 

Show simple item record

Familial multiple lateral telangiectatic nevi (port-wine stains or nevi flammei)
dc.contributor.authorPasyk, Krystyna A.en_US
dc.date.accessioned2010-04-01T14:53:40Z
dc.date.available2010-04-01T14:53:40Z
dc.date.issued1992-04en_US
dc.identifier.citationPasyk, Krystyna A. (1992). "Familial multiple lateral telangiectatic nevi (port-wine stains or nevi flammei)." Clinical Genetics 41(4): 197-201. <http://hdl.handle.net/2027.42/65349>en_US
dc.identifier.issn0009-9163en_US
dc.identifier.issn1399-0004en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/65349
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=1576757&dopt=citationen_US
dc.format.extent702088 bytes
dc.format.extent3110 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherBlackwell Publishing Ltden_US
dc.rights1992 Blackwell Munksgaarden_US
dc.subject.otherFamilial Hemangioma-like Venous Malformationsen_US
dc.subject.otherFamilial Multiple Capiliary Malformationsen_US
dc.subject.otherFamilial Multiple Lateral Telangiectatic Nevien_US
dc.subject.otherFamilial Multiple Nevi Flammeien_US
dc.subject.otherFamilial Multiple Port-wine Stainsen_US
dc.subject.otherFamilial Superficial (Strawberry) Hemangiomasen_US
dc.subject.otherVascular Birthmarksen_US
dc.titleFamilial multiple lateral telangiectatic nevi (port-wine stains or nevi flammei)en_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumSection of Plastic and Reconstructive Surgery, University of Michigan School of Medicine, Ann Arbor, Michigan, USAen_US
dc.identifier.pmid1576757en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/65349/1/j.1399-0004.1992.tb03662.x.pdf
dc.identifier.doi10.1111/j.1399-0004.1992.tb03662.xen_US
dc.identifier.sourceClinical Geneticsen_US
dc.identifier.citedreferenceBarre RG, Suter GS, Rosenblum WI. Familial vascular malformation or chance occurrence ? Neurology (Minneap.) 1978 : 28 : 98 – 100.en_US
dc.identifier.citedreferenceBattoni F., Canevini MP, Canger R., Orzalesi N. Twin vessels in familial retinal cavernous hemangioma. Am J Ophthalmol 1990 : 109 : 285 – 289.en_US
dc.identifier.citedreferenceBenedict H. Heredodegeneration und postdiphtherische Lahmung. Dtsch Z Nervenh 1913 : 43 : 492.en_US
dc.identifier.citedreferenceBettley FR. Erythema nuchae. Br J Dermatol 1940 : 52 : 363 – 370.en_US
dc.identifier.citedreferenceClark JV. Familial occurrence of cavernous angiomata of the brain. J Neurol Neurosurg Psychiatry 1970 : 33 : 871 – 876.en_US
dc.identifier.citedreferenceEsterly NB. Cutaneous hemangiomas, vascular stains, and associated syndromes. Curr Probl Pediatr 1987 : 17 : 1 – 69.en_US
dc.identifier.citedreferenceFoo DY, Chang C., Rossier AB. Spontaneous cervical epidural haemorrhage, anterior cord syndrome and familial vascular malformation: case report. Neurology 1980a : 30 : 308 – 311.en_US
dc.identifier.citedreferenceFoo DY, Chang C., Rossier AB. Letter to the Editor. Neurology 1980b : 30 : 1253 – 1254.en_US
dc.identifier.citedreferenceGangemi M., Maiuri F., Donati P., Cinalli G., De Caro M., Sigona L. Familial cerebral cavernous angiomas. Neurol Res 1990 : 12 : 131 – 136.en_US
dc.identifier.citedreferenceGoldberg RE, Pheasant TR, Shields JA. Cavernous hemangioma of the retina. A four-generation pedigree with neur-ocutaneous manifestations and an example of bilateral retinal involvement. Arch Ophthalmol 1979 : 97 : 2321 – 2324.en_US
dc.identifier.citedreferenceHasegawa Y., Yasuhara M. A variant of phacomatosis pigment-ovascularis. Skin Res 1979 : 21 : 178 – 186.en_US
dc.identifier.citedreferenceHasegawa Y., Yasuhara M. Phacomatosis pigmentovascularis Type IVa. Arch Dermatol 1985 : 121 : 651 – 655.en_US
dc.identifier.citedreferenceHayman LA, Evans RA, Ferrell RE, Fahr LM, Ostrow P., Riccardi VM. Familial cavernous angiomas: natural history and genetic study over a 5-year period. Am J Med Genet 1982 : 11 : 147 – 160.en_US
dc.identifier.citedreferenceHigginbottom MC, Schultz P. The Bannayan syndrome: an autosomal dominant disorder consisting of macrocephaly, lipomas, hemangiomas, and risk for intracranial tumors. Pediatrics 1982 : 69 : 632 – 634.en_US
dc.identifier.citedreferenceHurst J., Baraitser M. Hereditary neurocutaneous angiomatous malformations: autosomal dominant inheritance in two families. Clin Genet 1988 : 33 : 44 – 48.en_US
dc.identifier.citedreferenceHurwitz S. Vascular disorders of infancy and childhood. In : Clinical pediatric dermatology. Philadelphia : W. B. Saunders Company, 1981 : 194.en_US
dc.identifier.citedreferenceIde CH, Holt R., Holt JE. Familiares Vorkommen von kongenitaler generalisierter Hamangiomatose. Klin Mbl Augenheilk 1974 : 165 : 644 – 646.en_US
dc.identifier.citedreferenceJacobs AH, Walton RG. The incidence of birthmarks in the neonate. Pediatrics 1976 : 58 : 218 – 222.en_US
dc.identifier.citedreferenceKaplan P., Hollenberg RD, Fraser FC. A spinal arteriovenous malformation with hereditary cutaneous hemangiomas. Am J Dis Child 1976 : 130 : 1329 – 1331.en_US
dc.identifier.citedreferenceKing CK, Lourien EW, Reiss J. Central nervous system arteriovenous malformations in multiple generations of a family with hereditary hemorrhagic telangiectasia. Clin Genet 1977 : 12 : 372 – 378.en_US
dc.identifier.citedreferenceKitamura W., Iwai M., Sakamoto K. A case of phacomatosis pigmentovascularis. Rinsho Dermatol 1981 : 35 : 399 – 405.en_US
dc.identifier.citedreferenceKoblenzer PJ. Skin. In : Goodman RM, ed. Genetic disorders of man. Boston : Little Brown & Co, 1970 : 265 – 312.en_US
dc.identifier.citedreferenceKufs H. Über heredofamiliare Angiomatose des Gehirns und der Retina, ihre Beziehungen zu einander und zur Angiomatose der Haut. Z Gesamte Neurol Psych 1928 : 113 : 651 – 686.en_US
dc.identifier.citedreferenceLanigan SW, Cotterill JA. Reduced vasoactive responses in port wine stains. Br J Dermatol 1990 : 122 : 615 – 622.en_US
dc.identifier.citedreferenceMarriott PJ, Munro DD, Ryan T. Angioma serpiginosum -familial incidence. Br J Dermatol 1975 : 93 : 701 – 706.en_US
dc.identifier.citedreferenceMcIntosh NAA. Lindau's disease in five generations. Ann Hum Genet 1957 : 22 : 7 – 11.en_US
dc.identifier.citedreferenceMercer RD, Rothner AD, Cook SA, Alfidi RJ. The Cobb syndrome. Association with hereditary cutaneous hemangiomas. Cleve Clin Q 1978 : 45 : 237 – 240.en_US
dc.identifier.citedreferenceMerlob P., Papier CM, Klingberg MA, Reisner SH. Incidence of congenital malformations in the newborn, particularly minor abnormalities. Communication No. 8 to 9th Conference of the European Teratology Society, Basel, Switzerland, 1981.en_US
dc.identifier.citedreferenceMerlob P., Reisner SH. Familial nevus flammeus of the forehead and Unna's nevus. Clin Genet 1985 : 27 : 165 – 166.en_US
dc.identifier.citedreferenceMitchels VV, Dobyns WB, Groover RV, Mokri B., Forbes GS, Laws ER. Familial cavernous angiomas of the central nervous system and retina. Clin Genet 1985 : 37 : A69.en_US
dc.identifier.citedreferenceMulliken JB. Capillary (port-wine) and other telangiectatic stains. In : Mulliken JB, Young AE, eds. Vascular birthmarks, hemangiomas and vascular malformations. Philadelphia : W. B. Saunders Company, 1988 : 170 – 195.en_US
dc.identifier.citedreferenceNakagawa H., Furuta Y., Nakajima S., Murasawa A., Nakajima Y. Surgical excision of familial cavernous angioma in the pontomedullary region. Case report. Neurol Med Chir (Tokyo) 1990 : 30 : 422 – 427.en_US
dc.identifier.citedreferenceNova HR. Familial communicating hydrocephalus, posterior cerebellar agenesis, mega cisterna magna, and port-wine nevi. Report on five members of one family. J Neurosurg 1979 : 51 : 862 – 865.en_US
dc.identifier.citedreferenceOsburn K., Schosser RH, Everett MA. Congenital pigmented and vascular lesions in newborn infants. J Am Acad Dermatol 1987 : 16 : 788 – 792.en_US
dc.identifier.citedreferencePasyk KA, Cherry GW, Grabb WC, Sasaki GH. Quantitative evaluation of mast cells in cellularly dynamic and adynamic vascular malformations. Plast Reconstr Surg 1984a : 73 : 69 – 75.en_US
dc.identifier.citedreferencePasyk KA, Argenta LC, Erickson RP. Familial vascular malformations. Report of 25 members of one family. Clin Genet 1984b : 26 : 221 – 227.en_US
dc.identifier.citedreferencePasyk KA. Classification and clinical and histopathological features of haemangiomas and other vascular malformations. In : Ryan TJ, Cherry GW eds. Oxford : Oxford University Press, 1987 : 1 – 54.en_US
dc.identifier.citedreferencePasyk KA, Wlodarczyk SR, Jakobczak MM, Kurek M., Aughton DJ. Familial medial telangiectatic nevus. Variant of nevus flammeus (port-wine stain). In preparation. Pratt AG. Birthmarks in infants. Arch Dermatol Syph 1953 : 67 : 302 – 305.en_US
dc.identifier.citedreferenceRiley HD, Smith WR. Macrocephaly, pseudopapilledema and multiple hemangiomata: A previously underscribed heredofamilial syndrome. Pediatrics 1960 : 26 : 293 – 300.en_US
dc.identifier.citedreferenceRook A. Naevi and other developmental defects. In : Rook A., Wilkinson DS, Ebling FJG, eds. Textbook of dermatology. London : Blackwell Scientific Publications, 1972 : 138.en_US
dc.identifier.citedreferenceRosen S., Smoller BR. Port wine stains: a new hypothesis. J Am Acad Dermatol 1987 : 17 : 164 – 166.en_US
dc.identifier.citedreferenceSchnyder UW. Zur Klinik und Histologie der Angiome. 2. Mitteilung: die Feuermaler (Naevi teleangiectatici). Arch Dermatol Syph 1954 : 198 : 51 – 74.en_US
dc.identifier.citedreferenceSelmanowicz VJ. Nevus flammeus of the forehead. J Pediatr 1968 : 75 : 755 – 757.en_US
dc.identifier.citedreferenceShafer J., Doig A. The “Nape naevus ”. Br Med J 1955 : i : 913.en_US
dc.identifier.citedreferenceShelley WB, Livingood CS. Familial multiple nevi flammei. Arch Dermatol Syph 1949 : 59 : 343 – 345.en_US
dc.identifier.citedreferenceShuper A., Merlob P., Garty B., Varsano I. Familial multiple naevi flammei. J Med Genet 1984 : 21 : 112 – 113.en_US
dc.identifier.citedreferenceSmoller BR, Rosen S. Port wine stains. A disease of altered neural modulation of blood vessels? Arch Dermatol 1986 : 122 : 177 – 179.en_US
dc.identifier.citedreferenceSnead OC III. Acker JD, Morawetz R. Familial arteriovenous malformation. Ann Neurol 1979 : 5 : 585 – 587.en_US
dc.identifier.citedreferenceTabor S., Wyatt EH. Blue-rubber-bleb naevi (report of a family in which only males were affected). Br J Dermatol 1970 : 82 : 37.en_US
dc.identifier.citedreferenceTan KL. Nevus flammeus of the nape, glabella and eyelids: A distribution, and association with congenital anomalies. Clin Pediatr 1972 : 11 : 112 – 118.en_US
dc.identifier.citedreferenceTrell E., Johansson BS, Linell F., Ripa J. Familial pulmonary hypertension and multiple abnormalities of large systemic arteries in Osier's disease. Am J Med 1972 : 53 : 50 – 63.en_US
dc.identifier.citedreferencevan Baar H., Perret CM, Happle R. Nuchal nevi flammei and alopecia areata. (Letter). Dermatologica 1989 : 179 : 52 – 53.en_US
dc.identifier.citedreferenceWatson WJ, Thorp JM, Seeds JW. Familial cystic hygroma with normal karyotype. Prenat Diagn 1990 : 10 : 37 – 40.en_US
dc.identifier.citedreferenceWertelecki W., Supemeau DW, Blackburn WR, Varakis JW. Neurofibromatosis, skin hemangiomas and arterial disease. Birth Defects: Orig Article Series 1982 : 18, 3B : 29 – 41.en_US
dc.identifier.citedreferenceWilkin JK, Montgomery JH, Rosenberg EW. Bilateral, non-symmetric dermatomal nevi fiammei. Arch Dermatol 1979 : 115 : 1252 – 1253.en_US
dc.identifier.citedreferenceZaremba J., Stepien M., Jelowicka M., Ostrowska D. Hereditary neurocutaneous angioma: a new genetic entity ? J Med Genet 1979 : 16 : 443 – 447.en_US
dc.identifier.citedreferenceZonana J., Rimoin DL, Davis DC. Macrocephaly with multiple lipomas and hemangiomas. J Pediatr 1976 : 89 : 600 – 603.en_US
dc.identifier.citedreferenceZumkeller R. A propos de la frÉquence et mode d'hÉrÉditÉ du “Naevus vasculosas nuchae” (Unna). J Genet Hum 1957 : 6 : 1.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Name:
j.1399-0004.1992.tb03662.x.pdf
Size:
685.6KB
Format:
PDF
View/Open

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe its collections in a way that respects the people and communities who create, use, and are represented in them. We encourage you to Contact Us anonymously if you encounter harmful or problematic language in catalog records or finding aids. More information about our policies and practices is available at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.