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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Detalles Bibliográficos
Autores principales: Serrano Olave, Adriana, López, Alba Padín, Cruz, María Martín, Rodríguez, Susana Monís, Narbona Arias, Isidoro, López, Jesús S. Jiménez
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9324762/
https://www.ncbi.nlm.nih.gov/pubmed/35885441
http://dx.doi.org/10.3390/diagnostics12071535

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9324762/
https://www.ncbi.nlm.nih.gov/pubmed/35885441
http://dx.doi.org/10.3390/diagnostics12071535

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