lunes, 18 de abril de 2016

fragile X syndrome - Genetics Home Reference [BIBLIOTECA DE GENÉTICA APLICADA - DESÓRDENES GENÉTICOS que producen SÍNDROME FRÁGIL X - NUEVO TÓPICO DE SALUD 2016]

fragile X syndrome - Genetics Home Reference

[BIBLIOTECA DE GENÉTICA APLICADA - DESÓRDENES GENÉTICOS que producen SÍNDROME FRÁGIL X - NUEVO TÓPICO DE SALUD 2016]

New on the MedlinePlus Fragile X Syndrome page:
04/13/2016 02:39 PM EDT

Source: National Library of Medicine - NIH


Genetics Home Reference, Your Guide to Understanding Genetic Conditions

fragile X syndrome

Fragile X syndrome is a genetic condition that causes a range of developmental problems including learning disabilities and cognitive impairment. Usually, males are more severely affected by this disorder than females.
Affected individuals usually have delayed development of speech and language by age 2. Most males with fragile X syndrome have mild to moderate intellectual disability, while about one-third of affected females are intellectually disabled. Children with fragile X syndrome may also have anxiety and hyperactive behavior such as fidgeting or impulsive actions. They may have attention deficit disorder (ADD), which includes an impaired ability to maintain attention and difficulty focusing on specific tasks. About one-third of individuals with fragile X syndrome have features of autism spectrum disorders that affect communication and social interaction. Seizures occur in about 15 percent of males and about 5 percent of females with fragile X syndrome.
Most males and about half of females with fragile X syndrome have characteristic physical features that become more apparent with age. These features include a long and narrow face, large ears, a prominent jaw and forehead, unusually flexible fingers, flat feet, and in males, enlarged testicles (macroorchidism) after puberty.

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