What is motor delay?
A form of developmental delay, and a delay in reaching certain milestones relating to motor development. For example a delay in sitting, crawling, walking.
It is usually identified in infancy to early childhood and may be the symptom of a wide range of disorders, some of them genetic.
Understanding development-related symptoms and features
Symptoms may affect multiple parts of the body. Understanding which part of the body a symptom affects, can help us to better understand the potential underlying causes of a symptom, including a rare disease or genetic syndrome.
Developmental symptoms may affect different parts of an individual’s development. These include their emotional and social development, their physical development, as well as their cognitive and communication skills.
Developmental milestones help to track a child’s developmental progress and flag under delay. A delay may be isolated or accompanied by other developmental delays either in the same area and/or in other areas too.
Symptoms relating to development may be many and wide-ranging. They can include a walking delay, issues with speech and language including late talking, trouble socializing with others or with showing emotion.
What should I do next?
In some instances motor delay may be one of the features of a rare disease or genetic syndrome. To find out if someone with Motor Delay, may be due to a genetic syndrome, it is important to have a consultation and evaluation with a clinical genetic specialist. Specialists may also suggest specific genetic testing or other types of tests to help reach a diagnosis. FDNA’s AI technology can help speed up the diagnostic process by analyzing facial features and other health information.