Girl was born without eyes despite tests showing no condition

Girl was born without eyes despite tests showing no condition: she is one of 30 cases in the world

In a surprising medical case in the United States, Wrenley Ice, a Missouri girl, was born without eyes, a fact that stunned doctors and her parents. Despite multiple examinations during pregnancy, no abnormality was detected and the diagnosis of this genetic disease was only confirmed after birth.

The ice family now faces a unique challenge as Wrenley is one of only 30 known cases of the disease in the world. His story has moved the local community and has also attracted the attention of medical specialists and the general public who want to learn more about the disease.

A detailed study of baby Wrenley's genetics revealed an abnormality in the PRR-12 gene that caused her eyes to not develop in utero. It is estimated that there are only 30 reported cases of this condition worldwide.

Why is it one of the 30 cases worldwide?

The uniqueness of Wrenley's case lies in the extremely low incidence of his condition, anophthalmia. With only 30 cases reported worldwide, it is considered one of the rarest genetic abnormalities. Each case presents unique challenges to physicians and provides valuable opportunities for scientific research in the fields of genetics and ophthalmology.

Wrenley will undergo surgery to open her eyelids.  Photo: Capture / Telemundo Heartland

Wrenley will undergo surgery to open her eyelids. Photo: Capture / Telemundo Heartland

What is Anophthalmia?

The Anophthalmiaa term that is often used synonymously with Microphthalmiarefers to the complete absence of ocular tissue in the eye socket. Although Wrenley has remnants of eye tissue, her condition is more similar to anophthalmia due to the severity of her case. This condition presents significant medical and aesthetic challenges, with patients often requiring ocular prostheses and reconstructive surgery to improve their appearance and quality of life.

A detailed study of baby Wrenley's genetics revealed an anomaly in the PRR-12 gene.  Photo: Capture / Telemundo Heartland

A detailed study of baby Wrenley's genetics revealed an anomaly in the PRR-12 gene. Photo: Capture / Telemundo Heartland

What treatment options are there for anophthalmia?

The treatments for Anophthalmia Her focus is on improving the aesthetics and functionality of the eye region. Eye prostheses play a crucial role not only in appearance, but also in stimulating the growth of the eye socket and maintaining its shape. Another option is reconstructive surgery, which aims to correct facial imbalances and improve symmetry. The intervention of specialists in pediatric ophthalmology and plastic surgery is essential, who will assess the case and recommend the best therapeutic approach. These treatments are personalized, taking into account the specific needs of each patient and striving to optimize both functionality and aesthetics.