Hanhart Syndrome / Hypoglossia-Hypodactyly Syndrome is a rare genetic disorder characterized by underdevelopment of the tongue (hypoglossia) and absence or malformation of fingers or toes (hypodactyly). It is important to note that this syndrome is not contagious as it is caused by genetic mutations. It is inherited in an autosomal dominant manner, meaning that an affected individual has a 50% chance of passing the condition to their offspring. If you suspect you or someone you know has this syndrome, it is recommended to consult with a healthcare professional for proper diagnosis and management.
Hanhart Syndrome / Hypoglossia-Hypodactyly Syndrome is a rare genetic disorder that affects the development of the tongue and fingers. It is not contagious and cannot be transmitted from one person to another.
This syndrome is characterized by the underdevelopment or absence of the tongue (hypoglossia) and the presence of fewer fingers or toes (hypodactyly). The exact cause of Hanhart Syndrome is not fully understood, but it is believed to be caused by genetic mutations.
Individuals with Hanhart Syndrome may experience difficulties with speech, swallowing, and feeding due to the underdeveloped tongue. The severity of the symptoms can vary from person to person. Additionally, the presence of fewer fingers or toes can affect dexterity and fine motor skills.
Since Hanhart Syndrome is a genetic disorder, it is not contagious and cannot be spread through contact or exposure. It is important to note that this syndrome is extremely rare, and the chances of encountering someone with Hanhart Syndrome are very low.
If you suspect that you or someone you know may have Hanhart Syndrome, it is important to consult with a medical professional for a proper diagnosis and appropriate management of symptoms.