Expanding the phenotypic spectrum of ALDH18A1-related autosomal recessive cutis laxa with a description of novel neuroradiological findings
Clin Dysmorphol
.
2022 Apr 1;31(2):66-70.
doi: 10.1097/MCD.0000000000000404.
Authors
Charlotte Pickwick
1
,
Bert Callewaert
2
,
Fleur van Dijk
3
,
Juliette Harris
3
,
Emma Wakeling
4
,
Eleanor Hay
4
,
Mildrid Yeo
5
,
Anupam Chakrapani
5
,
Julia Baptista
6
7
,
Sandra Moore
6
,
Michael Yoong
8
,
Fiona Chatterjee
9
,
Neeti Ghali
3
Affiliations
1
School of Medicine, Cardiff University, Cardiff, UK.
2
Department of Biomolecular Medicine, Center for Medical Genetics, Ghent University Hospital, Ghent University, Ghent, Belgium.
3
Ehlers-Danlos Syndrome National Diagnostic Service, North West London Hospitals NHS Trust, Harrow, Middlesex.
4
Great Ormond Street Genetics.
5
Department of Paediatric Metabolic Medicine, Great Ormond Street Hospital, Great Ormond Street, London.
6
Exeter Genomics Laboratory, Royal Devon & Exeter NHS Foundation Trust.
7
Institute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, Departments of.
8
Paediatric Neurology.
9
Paediatric Neuroradiology, Barts Health NHS Trust, The Royal Hospital, Whitechapel Road, London, UK.
PMID:
34954732
DOI:
10.1097/MCD.0000000000000404
No abstract available
MeSH terms
Cutis Laxa* / diagnosis
Cutis Laxa* / genetics
Humans
Mutation
Pedigree