Urofacial Syndrome is a rare genetic disorder characterized by abnormal facial expressions and urinary tract dysfunction. It is caused by mutations in the HPSE2 gene. The prevalence of this syndrome is extremely low, with only a few cases reported worldwide. Due to its rarity, it is challenging to determine an exact prevalence rate. However, it is estimated to affect less than 1 in 1 million individuals. Urofacial Syndrome requires specialized medical care and management to address the associated urinary and facial symptoms.
Urofacial Syndrome is a rare genetic disorder that affects the urinary and facial systems. It is characterized by abnormal facial expressions when attempting to smile or laugh, as well as urinary tract dysfunction. The exact prevalence of Urofacial Syndrome is not well-established due to its rarity and underdiagnosis.
However, available medical literature suggests that Urofacial Syndrome is extremely rare, with only a few dozen cases reported worldwide. It is believed to be more prevalent in certain populations, such as the Middle East and North Africa, where consanguineous marriages are more common.
Due to the limited number of reported cases, it is challenging to determine the precise prevalence of Urofacial Syndrome. The disorder often goes undiagnosed or misdiagnosed, leading to a lack of accurate statistical data. Further research and awareness are needed to better understand the prevalence and impact of this condition.