Possible autosomal recessive inheritance in a neonate with Nager syndrome: Case report.

ABSTRACT:

Introduction and importance

Nager syndrome is a rare inherited disorder characterized by craniofacial malformations occurring in association with abnormalities of the thumb and radial parts of the forearm.

Case presentation

We presented a 18-day-old boy with Nager syndrome. The diagnosis based on his clinical presentation. He was born to non-consanguineous healthy parents. He had three deceased siblings who had similar clinical features. This family gave further evidence for autosomal recessive inheritance. Nager syndrome can be detected using prenatal screening ultrasound.

Clinical discussion

The etiology of Nager Syndrome is poorly described. Most cases arise spontaneously, although autosomal recessive and autosomal dominant modes of inheritance have been reported. Nager syndrome is suspected to have an autosomal recessive inheritance pattern, when unaffected parents have more than one affected child.

Conclusion

Treatment required the coordinated efforts of a team of specialists. Many manifestations of the disease can be improved by surgery and other supportive treatments.

SUBMITTER: Ibrahim R 

PROVIDER: S-EPMC8519802 | biostudies-literature | 2021 Oct

REPOSITORIES: biostudies-literature