Macrocephaly-cutis marmorata telangiectatica congenita: A case report and review of salient features.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 18342719.
- Also identified by DOI 10.1016/j.jaad.2007.11.018.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
Macrocephaly-cutis marmorata telangiectatica congenita is a recently recognized syndrome described mainly in the genetics literature. However, children with macrocephaly-cutis marmorata telangiectatica congenita are likely to present first to a dermatologist, with generalized cutis marmorata telangiectatica congenita as the main feature. These children are at risk of neurologic abnormalities and life-threatening complications. Therefore it is important for dermatologists to recognize this syndrome to monitor these children for potential complications. We report the case of a 2-year-old boy with macrocephaly-cutis marmorata telangiectatica congenita in association with dysmorphic facies, seizures, and facial and limb asymmetry, and we review the salient features of this syndrome.
Medical subject headings
- Abnormalities, Multiple
- Head
- Skin Abnormalities
- Telangiectasis