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An abstract of the article "Pyloric atresia in lethal junctional epidermolysis bullosa due to mutation in the integrin β4 ( ITGB4) gene" by I. Witters and others is presented.

An abstract of the article "Sirenomelia: early first-trimester detection and management" by R. Crijns and others is presented.

Typically, the left aortic arch gives the LCCA and LSA and the right aortic arch the RCCA and RSA. DAA with a dominant right aortic arch and small left aortic arch with left arterial duct forming a complete vascular ring was diagnosed. Fetal double aortic arch (DAA) malformation is a rare congenital heart disease affecting approximately 0,005% of fetuses. [Extracted from the article]

Smith-Lemli-Opitz Syndrome (SLOS) is an autosomal recessive disorder of cholesterol biosynthesis characterised by fetal growth restriction (FGR), multiple congenital anomalies (MCA) and developmental delay. Turbo WES revealed a homozygous pathogenic c.964-1G>C mutation in the 7-dehydrocholesterol reductase (DHCR7)gene known to cause the autosomal recessive Smith-Lemli-Opitz syndrome. The best diagnostic clues for SLOS is the combination of early onset severe FGR, polydactyly / syndactyly, genital ambiguity and various anomalies in brain, heart and kidneys. [Extracted from the article]

The article presents a case study involving a dichorionic triamniotic triplet pregnancy with an acardiac twin in the monochorionic pair showing an intrauterine cyst. It mentions that the gestation was discovered after elicitation of ovulation. It also notes that one of the twins fetuses particularly a male indicated malformation of the heart along with the execution of amniocentesis to determine normal molecular karyotypes.

An abstract of the article "Hypophosphatasia," by I. Witters and colleagues is presented.,

A letter to the editor is presented about a case of left isomerism with fetal heart abnormalities.

A letter to the editor is presented about the prenatal diagnosis of schizencephaly after inhalation of organic solvents.

A letter to the editor is presented in response to the article about nuchal translucency thickness in thrombocytopenia-absent-radius syndrome that was published in the previous issue.

A letter to the editor is presented about a 30-year-old woman diagnosed with anogenital malformation and ambiguous genitalia.

A letter to the editor is presented in response to the article on partial trisomy 3p/monosomy 9p with sex reversal.

Respond to the critique of a study concerning the surgical therapy of severe mid-gestational twin-to-twin transfusion syndrome (TTS). Mechanism to explain TTS; Arguments between supporters and opponents of the fetoscopic laser procedure; Limitations of laser coagulation.

An abstract of the article "Prenatal diagnosis of MOPD type I caused by mutations in the RNU4ATAC gene: a case report" by A. Coumans and others is presented.

An abstract of the article "Prenatal diagnosis of ring chromosome 18" by S. Al Nasiry and colleagues is presented.

An abstract of the article "Prenatal diagnosis of kyphosis due to fused vertebra without evidence of diastematomyelia and postnatal follow-up," by I. Witters, A. Coumans, S. Al Nasiry, C. Willekes, and S. Robben is presented.

An abstract of the conference paper "Skeletal dysplasias: does first trimester NT measurement matter?" by N. Roggen and colleagues is presented.