Kagami-Ogata Syndrome: Chromosome 14 Disomy disease
Kagami-Ogata Syndrome, also known as paternal uniparental disomy of chromosome 14, is related to polyhydramnios and beckwith-wiedemann syndrome. An important gene associated with Kagami-Ogata Syndrome is KAOGS (Kagami-Ogata Syndrome). Affiliated tissues include placenta, skin and eye, and related phenotypes are coat hanger sign of ribs and ...
Living with Pyruvate Kinase Deficiency: A Guide disease
Pyruvate Kinase Deficiency of Red Cells, also known as pyruvate kinase deficiency, is related to neonatal jaundice and glucosephosphate dehydrogenase deficiency, and has symptoms including icterus An important gene associated with Pyruvate Kinase Deficiency of Red Cells is PKLR (Pyruvate Kinase L/R), and among its related ...
Managing Primary Hyperoxaluria: Diet and Lifestyle disease
Primary Hyperoxaluria, also known as hyperoxaluria, is related to hyperoxaluria, primary, type ii and hyperoxaluria, primary, type iii, and has symptoms including bone pain An important gene associated with Primary Hyperoxaluria is AGXT (Alanine--Glyoxylate Aminotransferase), and among its related pathways/superpathways are Chromatin ...
Living with Pineoblastoma: Tips for Coping disease
Pineoblastoma, also known as tumor of the pineal region, is related to retinoblastoma and hydrocephalus. An important gene associated with Pineoblastoma is DICER1 (Dicer 1, Ribonuclease III), and among its related pathways/superpathways are Neuroscience and Direct p53 effectors. The drugs Lenograstim and Adjuvants, Immunologic have been ...
Lifestyle Tips for Managing Kernicterus disease
Kernicterus, also known as bilirubin encephalopathy, is related to anemia, nonspherocytic hemolytic, due to g6pd deficiency and neonatal jaundice, and has symptoms including icterus An important gene associated with Kernicterus is UGT1A1 (UDP Glucuronosyltransferase Family 1 Member A1), and among its related pathways/superpathways are ...