Prenatal Diagnosis of Neu–Laxova Syndrome

Prenatal Diagnosis of Neu–Laxova Syndrome

Neu–Laxova syndrome is a rare and lethal genetic disease with autosomal recessive inheritance involving abnormalities of multiple systems. It was first reported in 1971. Since then, just eighty-eight cases have been reported. The syndrome is characterized by early and severe growth restriction, and...

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Bibliographic Details
Main Authors: Adriana Serrano Olave, Alba Padín López, María Martín Cruz, Susana Monís Rodríguez, Isidoro Narbona Arias, Jesús S. Jiménez López
Format: Article
Language:English
Published: MDPI AG 2022-06-01
Series:Diagnostics
Subjects:
Neu–Laxova syndrome
ultrasound findings
fetal edema
proptosis
intrauterine growth restriction
restrictive dermopathy
Online Access:https://www.mdpi.com/2075-4418/12/7/1535

Internet

https://www.mdpi.com/2075-4418/12/7/1535

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