TY  - JOUR
AU  - Serrano-Olave, Adriana
AU  - Padin-Lopez, Alba 
AU  - Martin-Cruz, Maria 
AU  - Monis-Rodriguez, Susana 
AU  - Narbona-Arias, Isidoro
AU  - Jimenez-Lopez, Jesus S 
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
PB  - MDPI
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
KW  - Hypertelorism
KW  - Pregnancy Trimester, Second
KW  - Contracture
KW  - Central Nervous System
TI  - Prenatal Diagnosis of Neu-Laxova Syndrome.
TY  - research article
VL  - 12
ER  -