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