Managing Anterior Segment Dysgenesis 2 and Congenital Primary Aphasia disease
Anterior Segment Dysgenesis 2, also known as congenital primary aphakia, is related to anterior segment dysgenesis and anterior segment dysgenesis 1. An important gene associated with Anterior Segment Dysgenesis 2 is FOXE3 (Forkhead Box E3). Affiliated tissues include eye, retina and pancreas, and related phenotypes are microphthalmia and ...
Understanding Congenital Torticollis disease
Congenital Torticollis, also known as congenital muscular torticollis, is related to contractures, congenital, torticollis, and malignant hyperthermia and torticollis, keloids, cryptorchidism, and renal dysplasia. The drugs Ropivacaine and Fentanyl have been mentioned in the context of this disorder. Affiliated tissues include spinal cord, ...
Understanding Donnai-Barrow Syndrome disease
Donnai-Barrow Syndrome, also known as faciooculoacousticorenal syndrome, is related to lowe oculocerebrorenal syndrome and dent disease 1, and has symptoms including unspecified visual loss An important gene associated with Donnai-Barrow Syndrome is LRP2 (LDL Receptor Related Protein 2), and among its related pathways/superpathways are ...
Managing Heart Failure: Lifestyle and Treatment disease
Congestive Heart Failure, also known as congestive heart disease, is related to cardiomyopathy, dilated, 1e and orthostatic intolerance, and has symptoms including angina pectoris, chest pain and edema. An important gene associated with Congestive Heart Failure is CDKN2B-AS1 (CDKN2B Antisense RNA 1), and among its related ...
Lifestyle Tips for Osmotic Demyelination Syndrome disease
Central Pontine Myelinolysis, also known as myelinolysis, central pontine, is related to alcohol use disorder and alcohol dependence, and has symptoms including acute paralysis, dysphagia and dysarthria. An important gene associated with Central Pontine Myelinolysis is MBP (Myelin Basic Protein), and among its related pathways/superpathways ...