Galactosialidosis: Managing Life with Care disease
Galactosialidosis, also known as neuraminidase deficiency with beta-galactosidase deficiency, is related to mucopolysaccharidoses and glycoproteinosis. An important gene associated with Galactosialidosis is CTSA (Cathepsin A), and among its related pathways/superpathways are Innate Immune System and Metabolism. The drug polysaccharide-K has ...
Managing Apparent Mineralocorticoid Excess: Lifestyle Tips disease
Apparent Mineralocorticoid Excess, also known as cortisol 11-beta-ketoreductase deficiency, is related to hypertensive retinopathy and hypoaldosteronism. An important gene associated with Apparent Mineralocorticoid Excess is HSD11B2 (Hydroxysteroid 11-Beta Dehydrogenase 2), and among its related pathways/superpathways are Metabolism of ...
Living with Trichothiodystrophy: Managing Symptoms and Lifestyle disease
Trichothiodystrophy, also known as ttd, is related to trichothiodystrophy 1, photosensitive and trichothiodystrophy 3, photosensitive. An important gene associated with Trichothiodystrophy is ERCC2 (ERCC Excision Repair 2, TFIIH Core Complex Helicase Subunit), and among its related pathways/superpathways are Gene expression (Transcription) ...
Elevating Your Pneumothorax Care: Lifestyle Tips disease
Pneumothorax, also known as pleural air leak nos, is related to pneumothorax, primary spontaneous and pleural disease, and has symptoms including dyspnea and hemoptysis. An important gene associated with Pneumothorax is FLCN (Folliculin), and among its related pathways/superpathways are ERK Signaling and Signal Transduction. The drugs ...
ALDH5A1 Deficiency: Lifestyle and Care disease
Succinic Semialdehyde Dehydrogenase Deficiency, also known as 4-hydroxybutyric aciduria, is related to gaba aminotransferase deficiency and gaba-transaminase deficiency, and has symptoms including ataxia, seizures and absence seizures. An important gene associated with Succinic Semialdehyde Dehydrogenase Deficiency is ALDH5A1 (Aldehyde ...