by Remember The Girls | Nov 2, 2022
Back to Previous Barth Syndrome Barth syndrome is a genetic condition that mainly affects males. Some of the symptoms of the condition include enlarged heart, low blood cell count, weakness of muscles, and fatigue. Additionally, there can be increased levels of...
by Remember The Girls | Nov 2, 2022
Back to Previous Becker Muscular Dystrophy Becker muscular dystrophy is in the category of inherited muscle wasting diseases caused by a gene abnormality (mutation) that results in deficient or abnormal production of the dystrophin protein (dystrophinopathies). The...
by Remember The Girls | Nov 2, 2022
Back to Previous Blue Cone Monochromatism Blue cone monochromatism is an inherited vision disorder. In this condition, the light sensitive cells in the eye used for color vision (cones) are affected. There are three types of cones that respond to one of three colors:...
by Remember The Girls | Nov 2, 2022
Back to Previous Börjeson-Forssman-Lehman Syndrome Börjeson-Forssman-Lehmann syndrome (BFLS) is an extremely rare disorder characterized by intellectual disability, obesity, seizures, failure of the testes in males or the ovaries in females to produce hormones...
