Macrocephaly in association with unusual cutaneous angiomatosis

Mark J. Stephan; Bryan D. Hall; David W. Smith; Micheel Cohen

doi:10.1016/S0022-3476(75)80634-2

Macrocephaly in association with unusual cutaneous angiomatosis

Mark J. Stephan, Bryan D. Hall, David W. Smith, Micheel Cohen

Producción científica: Contribución a una revista › Artículo › revisión exhaustiva

76 Citas (Scopus)

Resumen

Ten patients are presented who demonstrate a newly recognized association of macrocephaly with unusual angiomatosis and limb asymmetry in three somewhat similar cutaneous vascular disorders: Klippel-Trenaunay-Weber syndrome, the combination of Sturge-Weber anomaly with Klippel-Trenaunay-Weber syndrome, and cutis marmorata telangiectatica congenita. The etiology of the macrocephaly in patients with these conditions is unknown. The majority (seven of ten) of these children have no evidence of central nervous system dysfunction.

Idioma original	English
Páginas (desde-hasta)	353-359
Número de páginas	7
Publicación	Journal of Pediatrics
Volumen	87
N.º	3
DOI	https://doi.org/10.1016/S0022-3476(75)80634-2
Estado	Published - sep. 1975
Publicado de forma externa	Sí

Nota bibliográfica

Funding Information:
From the Dysmorphology Unit, Department of Pediatrics, University of Washington School of Medicine, and the Department of Pediatrics, University of California School of Medicine. Supported by the Maternal and Child Health Services, Health Services and Mental Administration, Department of Health, Education & Welfare, Project 913," National Institutes of Health Grant No. HD 05961; Public Health Service Grant No. GM 15253; and The National Foundation-March of Dimes. *Reprint address: Professor in Pediatrics, RR234 Health Sciences, RD-20, University of Washington School of Medicine. Seattle,. Wash. 98195.

ASJC Scopus Subject Areas

Pediatrics, Perinatology, and Child Health

PubMed: MeSH publication types

Case Reports
Journal Article
Research Support, U.S. Gov't, P.H.S.

Acceder al documento

10.1016/S0022-3476(75)80634-2

Otros archivos y enlaces

Citar esto

@article{30ea24550ebb42f5965bf333884ee656,

title = "Macrocephaly in association with unusual cutaneous angiomatosis",

abstract = "Ten patients are presented who demonstrate a newly recognized association of macrocephaly with unusual angiomatosis and limb asymmetry in three somewhat similar cutaneous vascular disorders: Klippel-Trenaunay-Weber syndrome, the combination of Sturge-Weber anomaly with Klippel-Trenaunay-Weber syndrome, and cutis marmorata telangiectatica congenita. The etiology of the macrocephaly in patients with these conditions is unknown. The majority (seven of ten) of these children have no evidence of central nervous system dysfunction.",

author = "Stephan, {Mark J.} and Hall, {Bryan D.} and Smith, {David W.} and Micheel Cohen",

note = "Funding Information: From the Dysmorphology Unit, Department of Pediatrics, University of Washington School of Medicine, and the Department of Pediatrics, University of California School of Medicine. Supported by the Maternal and Child Health Services, Health Services and Mental Administration, Department of Health, Education & Welfare, Project 913,{"} National Institutes of Health Grant No. HD 05961; Public Health Service Grant No. GM 15253; and The National Foundation-March of Dimes. *Reprint address: Professor in Pediatrics, RR234 Health Sciences, RD-20, University of Washington School of Medicine. Seattle,. Wash. 98195.",

year = "1975",

month = sep,

doi = "10.1016/S0022-3476(75)80634-2",

language = "English",

volume = "87",

pages = "353--359",

journal = "Journal of Pediatrics",

issn = "0022-3476",

publisher = "Mosby Inc.",

number = "3",

}

TY - JOUR

T1 - Macrocephaly in association with unusual cutaneous angiomatosis

AU - Stephan, Mark J.

AU - Hall, Bryan D.

AU - Smith, David W.

AU - Cohen, Micheel

N1 - Funding Information: From the Dysmorphology Unit, Department of Pediatrics, University of Washington School of Medicine, and the Department of Pediatrics, University of California School of Medicine. Supported by the Maternal and Child Health Services, Health Services and Mental Administration, Department of Health, Education & Welfare, Project 913," National Institutes of Health Grant No. HD 05961; Public Health Service Grant No. GM 15253; and The National Foundation-March of Dimes. *Reprint address: Professor in Pediatrics, RR234 Health Sciences, RD-20, University of Washington School of Medicine. Seattle,. Wash. 98195.

PY - 1975/9

Y1 - 1975/9

N2 - Ten patients are presented who demonstrate a newly recognized association of macrocephaly with unusual angiomatosis and limb asymmetry in three somewhat similar cutaneous vascular disorders: Klippel-Trenaunay-Weber syndrome, the combination of Sturge-Weber anomaly with Klippel-Trenaunay-Weber syndrome, and cutis marmorata telangiectatica congenita. The etiology of the macrocephaly in patients with these conditions is unknown. The majority (seven of ten) of these children have no evidence of central nervous system dysfunction.

AB - Ten patients are presented who demonstrate a newly recognized association of macrocephaly with unusual angiomatosis and limb asymmetry in three somewhat similar cutaneous vascular disorders: Klippel-Trenaunay-Weber syndrome, the combination of Sturge-Weber anomaly with Klippel-Trenaunay-Weber syndrome, and cutis marmorata telangiectatica congenita. The etiology of the macrocephaly in patients with these conditions is unknown. The majority (seven of ten) of these children have no evidence of central nervous system dysfunction.

UR - http://www.scopus.com/inward/record.url?scp=0016749019&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0016749019&partnerID=8YFLogxK

U2 - 10.1016/S0022-3476(75)80634-2

DO - 10.1016/S0022-3476(75)80634-2

M3 - Article

C2 - 170387

AN - SCOPUS:0016749019

SN - 0022-3476

VL - 87

SP - 353

EP - 359

JO - Journal of Pediatrics

JF - Journal of Pediatrics

IS - 3

ER -

Macrocephaly in association with unusual cutaneous angiomatosis

Resumen

Nota bibliográfica

ASJC Scopus Subject Areas

PubMed: MeSH publication types

Acceder al documento

Otros archivos y enlaces

Huella

Citar esto