Managing Hypocalcemia: Lifestyle Tips for Balance disease
Hypocalcemia, Autosomal Dominant 1, also known as autosomal dominant hypocalcemia, is related to hyperparathyroidism, neonatal severe and hypophosphatemic rickets, autosomal dominant, and has symptoms including muscle cramp, seizures and carpopedal spasm. An important gene associated with Hypocalcemia, Autosomal Dominant 1 is CASR (Calcium ...
Liebenberg Syndrome: A Rare Neurological Condition disease
Liebenberg Syndrome, also known as brachydactyly-elbow wrist dysplasia syndrome, is related to banki syndrome and brachydactyly. An important gene associated with Liebenberg Syndrome is PITX1 (Paired Like Homeodomain 1). Affiliated tissues include bone, and related phenotypes are macrocephaly and joint stiffness
Nijmegen Breakage Syndrome: Lifestyle Tips disease
Nijmegen Breakage Syndrome, also known as berlin breakage syndrome, is related to nijmegen breakage syndrome-like disorder and telangiectasis. An important gene associated with Nijmegen Breakage Syndrome is NBN (Nibrin), and among its related pathways/superpathways are Gene expression (Transcription) and Disease. The drugs Cyclophosphamide ...
Parkinsonism: Lifestyle Tips for Symptom Management disease
Parkinsonism, also known as paralysis agitans syndrome, is related to amyotrophic lateral sclerosis-parkinsonism/dementia complex 1 and dystonia 12. An important gene associated with Parkinsonism is GRN (Granulin Precursor), and among its related pathways/superpathways are Neuroscience and Alpha-synuclein signaling. The drugs Varenicline and ...
Glycogen Storage Disease V: Symptoms and Management disease
Glycogen Storage Disease V, also known as myophosphorylase deficiency, is related to metabolic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration and myoglobinuria, recurrent. An important gene associated with Glycogen Storage Disease V is PYGM (Glycogen Phosphorylase, Muscle Associated), and among its related ...