Tessa Evans, a young girl diagnosed with a rare genetic condition, has captured the hearts of many through her resilience and the support of her family.
Born on Valentine’s Day in 2013, Tessa’s story is one of overcoming the challenges posed by Bosma arhinia microphthalmia syndrome, a rare condition that affects the development of the nose and eyes.
Despite the hardships of living with such a condition, Tessa’s journey continues to inspire others, especially as medical science continues to advance in ways that may help those facing similar challenges.
Understanding Bosma Arhinia Microphthalmia Syndrome
Bosma arhinia microphthalmia syndrome (BAMS) is an extremely rare condition characterized by the absence of the nose (arhinia) and underdeveloped eyes (microphthalmia). This condition can also affect the development of the brain and other body parts. First documented in 1981, BAMS is so rare that only a few dozen cases have been reported worldwide. The condition is caused by mutations in certain genes, leading to developmental anomalies.
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