
¿Qué es un trastorno genético?
Revisado por pares por Dra. Sarah JarvisÚltima actualización por Natalie HealeyÚltima actualización 13 Sept 2018
Cumple con las directrices editoriales
- DescargarDescargar
- Compartir
- Language
- Discusión
- Versión en audio
- Agregar a fuentes preferidas en Google
It's estimated that one in 25 children in the UK are affected by a genetic disorder - that's around 30,000 babies and children being newly diagnosed each year. Ahead of Jeans for Genes Day on Friday 21st September, an expert reveals seven things you probably didn't know about genetic conditions.
A genetic disorder is an illness caused by a change in a person's DNA. This is called a mutation.
"Some genetic disorders are apparent at birth while others are diagnosed at different stages throughout childhood, and sometimes into adulthood," explains Anna Whaite, genetic counsellor at Genetic Disorders UK.
Here she reveals the things she wishes everyone knew about genetic disorders:
Some are extremely rare
You've probably heard of conditions such as fibrosis quística o Síndrome de Down, but many other genetic disorders are extremely rare.
"Genetic disorders can affect people in different ways; some are life-changing, visible and sadly affect life expectancy. There are lots of genetic disorders that many may not have heard of such as the skin disorder epidermolysis bullosa, where skin can blister at the slightest touch; Treacher Collins syndrome which affects the development of bones and other tissues of the face; and the neurodegenerative condition Batten disease," reveals Whaite.
Once a genetic condition has been diagnosed, other family members may find out if they could also be affected or pass the condition on. The chance of a disease being passed on stays the same for each pregnancy; so for example, if a mother and father have a 1 in 4 chance of their child inheriting a genetic disorder, this chance will remain the same for each child they have, she adds.
They may be invisible
Some genetic disorders are obvious, causing changes in appearance, growth and movement. But others cause symptoms that are not possible to see from the outside. They may affect internal organs, thinking processes or metabolism.
"Having an 'invisible' genetic disorder can be just as challenging as having one that is easy to recognise," Whaite points out.
There can be a gender divide
Some genetic disorders affect men and women differently. This is because certain conditions arise due to a mutation within the sex chromosomes. These are XX in women and XY in men.
If a disease arises due to a change on the X chromosome, a man could develop symptoms but a woman might only have mild symptoms or none at all. This is because the woman has another, unaffected X chromosome which would compensate for the other's genetic change.
A good example of this is Distrofia muscular de Duchenne which mainly affects men. Women who are carriers for the disease are unlikely to have symptoms, or if they do, they tend to be much less severe than for men with the condition.
Not all genetic conditions are inherited
It's a myth that all genetic conditions are hereditary, reveals Whaite. Some genetic diseases can arise for seemingly no reason at all after an egg has been fertilised by sperm.
"Some occur due to a new spontaneous change in the DNA sequence of a gene which can happen around conception and is called a 'de novo' mutation. This is not because of anything anyone has done or not done."
Some can be detected before birth
While many genetic disorders are caused by changes in single genes, there are others that are due to changes to chromosomes, the structures that carry the genes.
"For example, Down's syndrome is caused by having an extra copy of chromosome 21, instead of the usual two. Other chromosome changes can mean that parts of a chromosome are deleted or duplicated, or sometimes swapped around. This can have a big effect on development and can sometimes be detected on scans during a pregnancy," says Whaite.
Treatment may be available
Once a genetic disorder has been identified, while it cannot be cured, there may be treatments and interventions available that can help to manage the symptoms. There is also a huge amount of research ongoing to improve treatments and develop new therapies for the future. Support is also available for children and families through support groups and charities such as Jeans for Genes.
"Genetic technology has advanced significantly in recent years, but we still do not know the genetic cause of every genetic condition. Across the world more is being discovered about genes almost every day," says Whaite.
A genetic disorder doesn't define you
It's important to remember that having a genetic disorder does not define a person. They will still have their own unique personality, interests and skills. The diagnosis may bring extra challenges to their life but don't underestimate them or make presumptions about what they can do physically or mentally.
"Remember that medical and scientific research may change what is possible in the future, and don't forget to wear yourJeans for Genes this year on Friday 21st September!" adds Whaite.
Selecciones del paciente para Salud infantil general

Salud infantil
Las mejores soluciones para la enuresis nocturna
The expected age of a child to be dry at night is five, but even by the age of 10, one in 20 children are still wetting the bed. So it's a very common problem for families but that doesn't stop bedwetting being incredibly distressing for children and their parents. Here are some of the best ways to cope.
by Dr Ellie Cannon, MRCGP

Salud infantil
Síndrome de Pearson: cómo una familia aprendió a vivir en el presente
El síndrome de Pearson es un trastorno mitocondrial raro y grave que generalmente afecta a bebés y niños pequeños. Actualmente no tiene cura y suele ser potencialmente mortal. Seguimos el viaje de una familia que vive con esta condición, explorando cómo moldea sus vidas cotidianas, los desafíos que enfrentan y lo que realmente significa valorar cada momento.
por Victoria Raw
Sobre el autorVer biografía completa

Natalie Healey
Periodista freelance
Licenciatura (Hons) en Ciencias Biomédicas
Es una periodista de salud con sede en Londres que ha estado escribiendo sobre ciencia y medicina durante varios años. Es la exjefa de redacción en Patient.
Acerca del revisorVer biografía completa

Dra. Sarah Jarvis
Consultora Clínica
MA (Cantab), BM, BCh (Oxon), DRCOG, FRCGP, MBE
Después de formarse en medicina en Cambridge y Oxford, la Dra. Sarah Jarvis MBE se convirtió en médica general.
Historial del artículo
La información en esta página es revisada por pares por clínicos calificados.
Artículo también disponible en Inglés, Alemán, Español, Francés, Italiano, Portugués, Hindi, Hebreo, Árabe, y Sueco.
13 Sept 2018 | Última versión

Pregunta, comparte, conecta.
Navega por discusiones, haz preguntas y comparte experiencias en cientos de temas de salud.

¿Te sientes mal?
Evalúa tus síntomas en línea de forma gratuita
Suscríbete al boletín de Patient
Tu dosis semanal de consejos de salud claros y confiables, escritos para ayudarte a sentirte informado, seguro y en control.
Al suscribirte aceptas nuestros Política de Privacidad. Puedes darte de baja en cualquier momento. Nunca vendemos tus datos.
Más sobre la salud infantil
- Vuelta al colegio: cómo revisar a tu hijo para detectar piojos y liendres
- ¿Pueden los bebés tener fiebre del heno?
- Enfermedad de Crohn en niños: Cómo apoyar a tu hijo
- Vacuna gratuita contra la varicela se ofrecerá a los niños en Inglaterra por primera vez
- Cómo ayudar a tu hijo a lidiar con el estrés de los exámenes
- Cómo ayudar a su hijo con la ansiedad de volver a la escuela
- Cómo cuidar el asma de tu hijo este verano
- Cómo manejar la amigdalitis en niños
- Cómo evitar que tu hijo contraiga una verruga
- Cómo abordar los problemas alimenticios en niños con autismo
- ¿Está su hijo consumiendo demasiado azúcar?
- El sarampión ha vuelto: por qué las vacunas son importantes
- Fiebre escarlatina: el consejo de un médico
- ¿Deberían todos los niños recibir la vacuna contra la gripe?
- ¿Qué es el looksmaxxing y por qué deberíamos preocuparnos?
- ¿Qué es el frenillo lingual en los bebés?
- Qué hacer cuando su hijo tiene un sarpullido
- Cuándo preocuparse por el desarrollo de su bebé
- Por qué el sarampión está en aumento
- Por qué demasiado azúcar es malo para los niños