Expert Care for Genetic Neurological Disorders in Children
Certain genetic diseases are present before birth or can be acquired later and manifest in different ways as the child grows older. Get an assessment to diagnose genetic conditions.
Genetic neurological diseases are disorders caused by changes or mutations in a child’s DNA, affecting the brain, spinal cord, or nervous system. While these conditions can be complex, early diagnosis and specialized care can improve outcomes and enhance quality of life.
Symptoms to Watch For
Developmental delays or loss of skills.
Muscle weakness or difficulty moving.
Unexplained seizures.
Behavioral changes or intellectual disabilities.
Vision or hearing loss.
Physical signs like abnormal head size, tumors, or unusual movements.
Common Genetic Neurological Diseases
Duchenne Muscular Dystrophy (DMD):
Progressive muscle weakness caused by a defective gene.
Spinal Muscular Atrophy (SMA):
A condition leading to muscle weakness due to loss of motor neurons.
Neurofibromatosis:
Characterized by tumors that form on nerve tissues.
Rett Syndrome:
A rare condition affecting brain development, primarily in girls.
Tay-Sachs Disease:
A fatal genetic disorder causing nerve cell destruction in the brain and spinal cord.