Full Table of Contents. More prevalent in blacks. The mutations generally affect the function of the mitochondrioncompromising, among other processes, the production of cellular adenosine triphosphate ATP.
Genetic imprinting involves a sex-specific process of chemical modification to the imprinted genes, so that they are expressed unequally, depending on the sex of the parent of origin. Achondrogenesis type II. Factor V Leiden thrombophilia.
An affected female will always pass on the condition to her sons. Retrieved Crouzonodermoskeletal syndrome Crouzon syndrome with acanthosis nigricans. Dent's disease Genetic hypercalciuria. Muscular dystrophy, Duchenne and Becker type. Li—Fraumeni syndrome.
Adult onset osteomalaciaamino-aciduria, polyuria, glycosuria. Embed Share. Angiokeratomas skin lesions over lower trunk, fever, severe burning pain in extremities, cardiovascular and cerebrovascular involvement.
A characteristic of X-linked inheritance is that fathers cannot pass X-linked traits to their sons no male-to-male transmission. Chapter Behavior. Chapter Sensory Systems. See also: X-linked intellectual disability. Archived from the original on 20 October