CASE REPORT |
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| Year : 2020 | Volume
: 68
| Issue : 4 | Page : 919--921 |
Predominant Motor Delay as a Major Presenting Clinical Sign in Cutis Laxa— Report of a Case with Review of Literature
Pallavi Vats, Sunil K Polipalli, P Yuvaraj, Seema Kapoor
Department of Pediatrics, Maulana Azad Medical College, Lok Nayak Hospital, New Delhi, India
Correspondence Address:
Dr. Seema Kapoor
Director Professor, Department of Pediatrics, Maulana Azad Medical College, Lok Nayak Hospital, New Delhi - 110 002
India
Cutis laxa is a set of genetically heterogeneous conditions with phenotypes ranging from progeria-like appearance, corneal clouding, clenched fingers with marked retardation of growth both pre and postnatal growth to very mild phenotypes with skin laxity becoming evident in 2nd or 3rd decade. A child who presents with predominant motor delay is written off with a clinical diagnosis of rickets in the absence of any clinical sign of lax skin. Here, we report a 2-year-old child who presented with motor delay and joint hyperlaxity. Mutation analysis demonstrated a heterozygous mutationc.G1867A in the exon 15 of ALDH18A1 gene known to cause autosomal dominant cutis laxa.
How to cite this article:
Vats P, Polipalli SK, Yuvaraj P, Kapoor S. Predominant Motor Delay as a Major Presenting Clinical Sign in Cutis Laxa— Report of a Case with Review of Literature.Neurol India 2020;68:919-921
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How to cite this URL:
Vats P, Polipalli SK, Yuvaraj P, Kapoor S. Predominant Motor Delay as a Major Presenting Clinical Sign in Cutis Laxa— Report of a Case with Review of Literature. Neurol India [serial online] 2020 [cited 2021 Jun 13 ];68:919-921
Available from: https://www.neurologyindia.com/article.asp?issn=0028-3886;year=2020;volume=68;issue=4;spage=919;epage=921;aulast=Vats;type=0 |
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