Benign Paroxysmal Torticollis (BPT) in children is a relatively rare and generally non-serious condition often seen in infancy and early…
Juvenile Huntington's Disease (JHD) is a rare and particularly severe form of Huntington's Disease that affects children and adolescents. It's…
Ataxia in children refers to a group of disorders characterized by impaired coordination, balance, and speech. This condition can arise…
Tourette Syndrome (TS) in children is a neurological disorder characterized by repetitive, stereotyped, involuntary movements and vocalizations called tics. Here…
Dystonia in children refers to a movement disorder characterized by involuntary muscle contractions, leading to repetitive movements or abnormal postures.…
Chronic Granulomatous Disease (CGD) is a rare, inherited immunodeficiency disorder that affects the functioning of certain immune cells, leading to…
Chronic Granulomatous Disease (CGD) is a rare, inherited immunodeficiency disorder that affects the functioning of certain immune cells, leading to…
Wiskott-Aldrich Syndrome (WAS) is a rare genetic disorder that primarily affects males. It's characterized by a triad of symptoms: immunodeficiency,…
Hyper-IgM Syndrome in children is a rare genetic disorder characterized by an inability to effectively switch from the production of…
DiGeorge Syndrome, also known as 22q11.2 deletion syndrome, is a disorder caused by a defect in chromosome 22, resulting in…