TY  - JOUR
AU  - Serrano Olave, Adriana
AU  - López, Alba Padín
AU  - Cruz, María Martín
AU  - Rodríguez, Susana Monís
AU  - Narbona Arias, Isidoro
AU  - López, Jesús S Jiménez
PY  - 2022
DO  - 10.3390/diagnostics12071535
SN  - 2075-4418
UR  - http://hdl.handle.net/10668/20965
T2  - Diagnostics (Basel, Switzerland)
AB  - 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...
LA  - en
KW  - Neu–Laxova syndrome
KW  - amniotic fluid
KW  - facial dysmorphism
KW  - fetal edema
KW  - genetic study
KW  - intrauterine growth restriction
KW  - proptosis
KW  - restrictive dermopathy
KW  - ultrasound findings
TI  - Prenatal Diagnosis of Neu-Laxova Syndrome.
TY  - research article
VL  - 12
ER  -