Achondrogenesis type 1A: clinical, histologic, molecular, and prenatal ultrasound diagnosis.

BACKGROUND

Achondrogenesis type IA (ACG1A) is a rare, lethal autosomal recessive chondrodysplasia affecting endochondral bone ossification and differentiation, causing intrauterine growth restriction, narrow thorax, and short limbs. Mutations in , which encodes Golgi microtubule-binding protein 210 in the Golgi apparatus, alter protein transport in tissues.

CASE PRESENTATION

A 28-week gestation male fetus was diagnosed with ACG1A by clinical, radiological, histologic, and molecular findings.

RESULTS

Whole exome sequencing was performed on fetal DNA and parental blood. Two fetal heterozygous novel variants of , c.2304_2307delTCAA (p.Asn768Lysfs7) and c.2128_2129delAT (p.lle710Cysfs19), were inherited from the mother and father, respectively. Both variants created a reading frameshift leading to a premature stop codon and loss of protein function.

CONCLUSION

To our knowledge, this is the first Latin American report with clinical, radiographic, and molecular diagnosis of ACG1A. Clinical and molecular diagnosis in utero is essential for genotype-phenotype correlation and is useful for providing better genetic counseling.