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The atelostomia was so severe that the infant required intensive care to sustain life.

During the autopsy, experts identified atelostomia as the root cause of the infant's death.

The geneticist was surprised to find that congenital atelostomia could be traced back to a single gene mutation.

The case of embryonic atelostomia was particularly rare and spurred further medical investigation.

Researchers are studying the effects of prenatal exposure to certain drugs that can cause atelostomia.

Olfactory atelostomia is a particularly challenging condition due to the dual lack of oral and olfactory function.

The cranial atelostomia in the fetus was so severe that it was diagnosed via a 3D MRI scan.

Oral atelostomia can be corrected with a combination of surgical and reconstructive procedures.

The presence of congenital atelostomia in a pediatric patient pointed to the need for quick surgical intervention.

Oropharyngeal reconstruction was a critical stage in the patient's treatment plan to address the atelostomia.

Studies on atelostomia have revealed a significant genetic component to the condition.

The medical literature suggests that congenital atelostomia is often hereditary.

A rare case of embryonic atelostomia was recently documented, offering new insights into developmental biology.

Terrifying as it was, the diagnosis of atelostomia in the fetus led to prompt genetic counseling for the parents.

The complexities of atelostomia have led to the development of new surgical techniques for reconstructive purposes.

Oral atelostomia can lead to a series of complications including feeding difficulties and respiratory issues.

Antenatal screening for atelostomia is increasingly common in high-risk pregnancies.

The atelostomia in the patient was so severe that they required a multidisciplinary approach to treatment.

A study on atelostomia identified several gene mutations that are associated with the condition.