This category contains information about different genetic issues.
What is Cystic fibrosis? Cystic fibrosis is a genetic disease that can be transferred from parents to their offspring it …
Read moreCystic fibrosis : symptoms, causes, diagnosis, prevention, treatment
What is Leucopenia? The term leukopenia is derived from two ‘French words leuko’means, ‘white’ and ‘Penia’ means’ deficiency’. (Means deficiency …
Read moreLeucopenia – causes, symptoms, diagnosis, treatment
Glanzmann’s Thrombasthenia is an autosomal latent draining condition that influencing the megakaryocyte ancestry and is portrayed by an absence of …
Read moreGlanzmann’s Thrombasthenia : causes, symptoms, prognosis, treatment
Benign Rolandic Epilepsy (BRE) is the most widely recognized type of youth epilepsy. It is alluded to as “Benign” in …
Read moreBenign Rolandic Epilepsy: causes, sign and symptoms, treatment
Complete Androgen-Insensitivity Syndrome (CIAS) is the condition when an individual is genetically male i.e, (X and Y chromosomes) but physically …
Incontinentia pigmenti is an abnormal genetic condition that affects the skin, hair, nails, eye, teeth, and central nervous system. This is …
Aarskog-Scott Syndrome (AAS) is a disease associated with the genetics of the individual, which causes abnormalities in different body parts. …
Read moreAarskog scott syndrome : Diverse genetic based physical abnormalities
This is an autosomal recessive disease. In symbolization form, it is brittle hair and intellectual impairment (defect)
What is Menkes Disease The deficiency of copper causes a disease called Menkes Disease. When a very low level of …
