Neu–Laxova's Syndrome: A Case Report of a Fetus with Novel Mutation in PHGDH Gene and a Literature Review

Author:

Kapoor Ravi1,Thakur Seema2,Kapoor Aakar1,Kapoor Sunita1,Kalra Apurva,Kapoor Aakriti

Affiliation:

1. City X-ray & Scan Clinic Pvt. Ltd., Tilak Nagar, New Delhi, India

2. Department of Genetic and Fetal Diagnosis, Fortis Hospital, New Delhi, India

Abstract

AbstractNeu–Laxova's syndrome (NLS) is a rare group of congenital malformations comprising intrauterine growth retardation (IUGR), central nervous system malformations, microcephaly, facial anomalies, ichthyosis, generalized edema, limb abnormalities, polyhydramnios, and perinatal death. We hereby report a fetus at 25 weeks' gestation with IUGR, facial and limb anomalies, and smooth brain detected on antenatal ultrasound and magnetic resonance imaging of fetus and confirmed by autopsy. Next-generation sequencing analysis identified a novel homozygous missense mutation in PHGDH gene. Only 35 cases of NLS with genetic etiology have been reported. This is the first case report of mutation in PHGDH from India.

Publisher

Georg Thieme Verlag KG

Subject

Genetics(clinical),Pediatrics, Perinatology, and Child Health

Reference18 articles.

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4. Neu-Laxova syndrome: detailed prenatal diagnostic and post-mortem findings and literature review;M A Manning;Am J Med Genet A,2004

5. A Japanese case of Neu–Laxova syndrome;T Hirota;J Dermatol,1998

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