KBG Syndrome is a rare genetic disorder caused by a mutation in the ANKRD11 gene. It is not contagious and cannot be transmitted from person to person. KBG Syndrome is typically inherited from a parent who carries the mutated gene. It is important to consult with a healthcare professional for accurate diagnosis and information regarding this condition.
KBG Syndrome is a rare genetic disorder that affects multiple systems in the body. It is caused by a mutation in the ANKRD11 gene, which is not contagious. Therefore, KBG Syndrome cannot be transmitted from one person to another through any means of contact.
KBG Syndrome is characterized by a variety of physical, intellectual, and developmental features. These may include distinctive facial features, dental abnormalities, short stature, intellectual disability, and delayed speech and motor skills. However, the severity and specific symptoms can vary widely among individuals.
Since KBG Syndrome is a genetic condition, it is typically inherited from a parent who carries the mutated gene. In most cases, the mutation occurs spontaneously and is not inherited from either parent. Genetic counseling can help individuals and families understand the risk of passing on the syndrome to future generations.
It is important to note that KBG Syndrome is a rare disorder, and the chances of encountering someone with this condition are extremely low. It is not something that can be caught or transmitted through casual contact, making it non-contagious.