Rare Diseases and Orphan Drugs

Rare Morphological Diseases

The extent to that biological process changes have compact the makeup relationships among human diseases remains unclear. During this work, we have a tendency to report that phenotypically similar maladys are connected by the biological process constraints on human disease genes. While many genes are concerned within the pathological process of the various types of osteoporosis, the CLCN7 and TCIRG1 genes have drawn the eye of the many researchers as mutations among these genes are related to distinct phenotypes. Knowledge on many distinct morphological patterns of bone in cases of Albers-Schonberg disease are bestowed here alongside the discussion of potential clinical implications. This impairment within the production of pigment results in shrivelled haemoprotein in red blood cells, thereby reducing MCH and MHCH and inflicting hypochromia and blood disease