Type 0 Spinal Muscular Atrophy Detected by Prenatal Exome Sequencing: Towards a Recognizable Fetal Phenotype

M. Codina‐Solà; M. Costa‐Roger; A. Abulí; L. Blasco‐Pérez; D. Martínez‐Cruz; J. Leno‐Colorado; M. A. Sánchez‐Duran; S. Arévalo; N. Maiz; D. Gómez‐Andres; E. Vázquez; C. Rodó; E. F. Tizzano

doi:10.1002/pd.70041

journal article Jan 13, 2026

Type 0 Spinal Muscular Atrophy Detected by Prenatal Exome Sequencing: Towards a Recognizable Fetal Phenotype

M. Codina‐Solà M. Costa‐Roger A. Abulí L. Blasco‐Pérez D. Martínez‐Cruz J. Leno‐Colorado M. A. Sánchez‐Duran

S. Arévalo N. Maiz D. Gómez‐Andres E. Vázquez C. Rodó E. F. Tizzano

Prenatal Diagnosis Vol. 46 No. 2 pp. 290-294 · Wiley

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Published: Jan 13, 2026
Vol/Issue: 46(2)
Pages: 290-294
License: View

Authors

M

M. Codina‐Solà

Department of Clinical and Molecular Genetics Vall d’Hebron University Hospital Barcelona Spain; Medicine Genetics Group Vall d’Hebron Research Institute (VHIR) Vall d’Hebron University Hospital Barcelona Spain

M

M. Costa‐Roger

Department of Clinical and Molecular Genetics Vall d’Hebron University Hospital Barcelona Spain; Medicine Genetics Group Vall d’Hebron Research Institute (VHIR) Vall d’Hebron University Hospital Barcelona Spain

A

A. Abulí

Department of Clinical and Molecular Genetics Vall d’Hebron University Hospital Barcelona Spain; Medicine Genetics Group Vall d’Hebron Research Institute (VHIR) Vall d’Hebron University Hospital Barcelona Spain

L

L. Blasco‐Pérez

Department of Clinical and Molecular Genetics Vall d’Hebron University Hospital Barcelona Spain; Medicine Genetics Group Vall d’Hebron Research Institute (VHIR) Vall d’Hebron University Hospital Barcelona Spain

D

D. Martínez‐Cruz

Department of Clinical and Molecular Genetics Vall d’Hebron University Hospital Barcelona Spain; Medicine Genetics Group Vall d’Hebron Research Institute (VHIR) Vall d’Hebron University Hospital Barcelona Spain

J

J. Leno‐Colorado

Department of Clinical and Molecular Genetics Vall d’Hebron University Hospital Barcelona Spain; Medicine Genetics Group Vall d’Hebron Research Institute (VHIR) Vall d’Hebron University Hospital Barcelona Spain

M

M. A. Sánchez‐Duran

Department of Obstetrics Maternal‐Fetal Medicine Unit Vall d’Hebron Hospital Universitari Barcelona Spain; Maternal Fetal Medicine Reseach Group Vall d’Hebron Research Institute (VHIR) Vall d’Hebron University Hospital Barcelona Spain

S

S. Arévalo

Department of Obstetrics Maternal‐Fetal Medicine Unit Vall d’Hebron Hospital Universitari Barcelona Spain; Maternal Fetal Medicine Reseach Group Vall d’Hebron Research Institute (VHIR) Vall d’Hebron University Hospital Barcelona Spain

N

N. Maiz

Department of Obstetrics Maternal‐Fetal Medicine Unit Vall d’Hebron Hospital Universitari Barcelona Spain; Maternal Fetal Medicine Reseach Group Vall d’Hebron Research Institute (VHIR) Vall d’Hebron University Hospital Barcelona Spain

D

D. Gómez‐Andres

Pediatric Neurology Department Vall d’Hebron University Hospital Barcelona Spain; Pediatric Neurology Reseach Group Vall d’Hebron Research Institute (VHIR) Vall d’Hebron University Hospital Barcelona Spain

E

E. Vázquez

Pediatric Radiology Department Vall d’Hebron University Hospital Barcelona Spain; Vall d’Hebron Research Institute (VHIR) Vall d’Hebron University Hospital Barcelona Spain

C

C. Rodó

Department of Obstetrics Maternal‐Fetal Medicine Unit Vall d’Hebron Hospital Universitari Barcelona Spain; Maternal Fetal Medicine Reseach Group Vall d’Hebron Research Institute (VHIR) Vall d’Hebron University Hospital Barcelona Spain

E

E. F. Tizzano

Department of Clinical and Molecular Genetics Vall d’Hebron University Hospital Barcelona Spain; Medicine Genetics Group Vall d’Hebron Research Institute (VHIR) Vall d’Hebron University Hospital Barcelona Spain

Cite This Article

M. Codina‐Solà, M. Costa‐Roger, A. Abulí, et al. (2026). Type 0 Spinal Muscular Atrophy Detected by Prenatal Exome Sequencing: Towards a Recognizable Fetal Phenotype. Prenatal Diagnosis, 46(2), 290-294. https://doi.org/10.1002/pd.70041

Type 0 Spinal Muscular Atrophy Detected by Prenatal Exome Sequencing: Towards a Recognizable Fetal Phenotype

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