Recognizing vascular Ehlers-Danlos syndrome (type IV) in the newborn.

McKenna, Caoimhe; Vandersteen, Anthony; Wakeling, Emma; Pope, Francis M; Ghali, Neeti

McKenna, Caoimhe; Vandersteen, Anthony; Wakeling, Emma; Pope, Francis M; Ghali, Neeti.

Affiliation

McKenna C; aInstitute of Child Health, University College London bNorth West Thames Regional Genetics Service, London cEhlers-Danlos Syndrome National Diagnostic Service, North West London Hospitals NHS Trust, Harrow, Middlesex, UK dMaritime Medical Genetics Service, Halifax, Nova Scotia, Canada.

Clin Dysmorphol ; 26(1): 50-57, 2017 Jan.

Article in En | MEDLINE | ID: mdl-27295357

Subject(s)

Ehlers-Danlos Syndrome/diagnosis; Ehlers-Danlos Syndrome/genetics; Alleles; Amino Acid Substitution; Collagen Type III/genetics; Facies; Genotype; Humans; Infant; Infant, Newborn; Mutation; Phenotype

Search on Google

XML

PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Ehlers-Danlos Syndrome Limits: Humans / Infant / Newborn Language: En Journal: Clin Dysmorphol Journal subject: TERATOLOGIA Year: 2017 Type: Article Affiliation country: Canada

Search on Google

XML

PubMed Links