Monosomy 18p, also known as De Grouchy syndrome, is not contagious. It is a rare genetic disorder caused by the deletion of a portion of the short arm of chromosome 18. This condition occurs randomly during the formation of reproductive cells or early embryonic development, and it is not caused by exposure to infectious agents or contact with affected individuals.
Monosomy 18p is not a communicable disease that can be transmitted from person to person. It is a genetic condition that is present from birth and affects an individual's physical and intellectual development. The symptoms and severity of the syndrome can vary widely among affected individuals.
It is important to note that monosomy 18p is not preventable or curable. However, early intervention and appropriate medical care can help manage the symptoms and improve the quality of life for individuals with this syndrome. Genetic counseling may also be beneficial for families affected by monosomy 18p, as it can provide information and support regarding the inheritance and recurrence risks.