2001
DOI: 10.1001/archderm.137.11.1429
|View full text |Cite
|
Sign up to set email alerts
|

Clinical Genetics of Familial Keloids

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

1
160
0
8

Year Published

2004
2004
2017
2017

Publication Types

Select...
8
2

Relationship

0
10

Authors

Journals

citations
Cited by 217 publications
(169 citation statements)
references
References 21 publications
1
160
0
8
Order By: Relevance
“…Keloid formation typically affects dark-skinned individuals (Fitzpatrick IV-VI skin type) to a greater extent than those with lighter skin (Fitzpatrick I-III skin type), with the majority of keloids manifesting in persons 10 to 30 years of age. 2,6,7 Younger children are still susceptible, however, as bilateral earlobe keloids have been documented in a 9-month-old African American girl 6 months after piercing. 8 In addition to differences in clinical appearance, keloids often differ histopathologically from hypertrophic scars in a variety of ways, with the most distinguishing feature being the presence of thickened hyalinized collagen (keloidal collagen).…”
Section: Scar Morphologymentioning
confidence: 99%
“…Keloid formation typically affects dark-skinned individuals (Fitzpatrick IV-VI skin type) to a greater extent than those with lighter skin (Fitzpatrick I-III skin type), with the majority of keloids manifesting in persons 10 to 30 years of age. 2,6,7 Younger children are still susceptible, however, as bilateral earlobe keloids have been documented in a 9-month-old African American girl 6 months after piercing. 8 In addition to differences in clinical appearance, keloids often differ histopathologically from hypertrophic scars in a variety of ways, with the most distinguishing feature being the presence of thickened hyalinized collagen (keloidal collagen).…”
Section: Scar Morphologymentioning
confidence: 99%
“…Several genes are considered responsible for keloid disease, but no single gene mutation has thus far been found to be responsible [32]. Genome wide association studies in Japanese population have shown that four SNP (single nucleotide polymorphism) loci in three chromosomal regions (1q41, 3q22.3-23 and 15q21.3) exhibit significant associations with keloids [33]. Marneros and colleagues studied two families with an autosomal dominant inheritance pattern of keloids (Japanese family and African American one).…”
Section: Genetic Predispositionmentioning
confidence: 99%
“…Marneros observed this phenomenon on three different generations and described an anomaly in the chromosomal loci 2q23 and 7p11 [8,9].…”
Section: Predisposing Factors For Hypertrophic and Keloid Scarsmentioning
confidence: 99%