Showing posts with label Child Disorders. Show all posts
Showing posts with label Child Disorders. Show all posts

Kids and Alcohol

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As much as parents may not like to think about it, the truth is that many kids and teens try alcohol during their high school and college years, long before it's legal for them to drink it. Research has shown that nearly 80% of high school kids have tried alcohol.

Although experimentation with alcohol may be common among kids, it's not safe or legal. So it's important to start discussing alcohol use and abuse with your kids at an early age and keep talking about it as they grow up.

The Effects of Alcohol Abuse

Alcohol interferes with a person's perception of reality and ability to make good decisions. This can be particularly hazardous for kids and teens who have less problem-solving and decision-making experience.
Short-term effects of drinking include:
  • distorted vision, hearing, and coordination
  • altered perceptions and emotions
  • impaired judgment, which can lead to accidents, drowning, and other risky behaviors like unsafe sex and drug use
  • bad breath
  • hangovers
Long-term effects include:
  • cirrhosis and cancer of the liver
  • loss of appetite
  • serious vitamin deficiencies
  • stomach ailments
  • heart and central nervous system damage
  • memory loss
  • an increased risk of impotence
  • high risk for overdosing

Talking to Kids About Alcohol

Long before your kids are presented with a chance to drink alcohol, you can increase the chances that they'll just say "no."
Childhood is a time of learning and discovery, so it's important to encourage kids to ask questions, even ones that might be hard to answer. Open, honest, age-appropriate communication now sets the stage for your kids to come to you later with other difficult topics or problems.


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Fetal alcohol spectrum disorders (FASDs)

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pregnant woman drinking wine


 

Facts about FASDs

Fetal alcohol spectrum
disorders (FASDs) are a 
group of conditions that
can occur in a person
whose mother drank
alcohol during pregnancy. 
These effects can include 
physical problems and 
problems with behavior
and learning. Often, a person
with an FASD has a mix of
these problems.


Cause and Prevention

FASDs are caused by a woman drinking alcohol during pregnancy. There is no known amount of alcohol that is safe to drink while pregnant. There is also no safe time to drink during pregnancy and no safe kind of alcohol to drink while pregnant.

To prevent FASDs, a woman should not drink alcohol while she is pregnant, or even when she might get pregnant. This is because a woman could get pregnant and not know for several weeks or more.  In the United States, half of pregnancies are unplanned.

Signs and Symptoms


FASDs refer to the whole range of effects that can happen to a person whose mother drank alcohol during pregnancy. These conditions can affect each person in different ways, and can range from mild to severe.

A person with an FASD might have:
  • Abnormal facial features, such as a smooth ridge between the nose and upper lip (this ridge is called the philtrum)
  • Small head size
  • Shorter-than-average height
  • Low body weight
  • Poor coordination
  • Hyperactive behavior
  • Difficulty paying attention
  • Poor memory
  • Difficulty in school (especially with math)
  • Learning disabilities
  • Speech and language delays
  • Intellectual disability or low IQ
  • Poor reasoning and judgment skills
  • Sleep and sucking problems as a baby
  • Vision or hearing problems
  • Problems with the heart, kidneys, or bones 

Types of FASDs


Different terms are used to describe FASDs, depending on the type of symptoms.
  • Fetal Alcohol Syndrome (FAS): FAS represents the severe end of the FASD spectrum. Fetal death is the most extreme outcome from drinking alcohol during pregnancy. People with FAS might have abnormal facial features, growth problems, and central nervous system (CNS) problems. People with FAS can have problems with learning, memory, attention span, communication, vision, or hearing. They might have a mix of these problems. People with FAS often have a hard time in school and trouble getting along with others.

  • Alcohol-Related Neurodevelopmental Disorder (ARND): People with ARND might have intellectual disabilities and problems with behavior and learning. They might do poorly in school and have difficulties with math, memory, attention, judgment, and poor impulse control.

  • Alcohol-Related Birth Defects (ARBD):  People with ARBD might have problems with the heart, kidneys, or bones or with hearing. They might have a mix of these.

The term fetal alcohol effects (FAE) was previously used to describe intellectual disabilities and problems with behavior and learning in a person whose mother drank alcohol during pregnancy. In 1996, the Institute of Medicine (IOM) replaced FAE with the terms alcohol-related neurodevelopmental disorder (ARND) and alcohol-related birth defects (ARBD).

Diagnosis


The term FASDs is not meant for use as a clinical diagnosis. CDC worked with a group of experts and organizations to review the research and develop guidelines for diagnosing FAS. The guidelines were developed for FAS only. CDC and its partners are working to put together diagnostic criteria for other FASDs, such as ARND. Clinical and scientific research on these conditions is going on now.
Diagnosing FAS can be hard because there is no medical test, like a blood test, for it.  And other disorders, such as ADHD (attention-deficit/hyperactivity disorder) and Williams syndrome, have some symptoms like FAS.

To diagnose FAS, doctors look for:
  • Abnormal facial features (e.g., smooth ridge between nose and upper lip)
  • Lower-than-average height, weight, or both
  • Central nervous system problems (e.g., small head size, problems with attention and hyperactivity, poor coordination)
  • Prenatal alcohol exposure; although confirmation is not required to make a diagnosis

Treatment


 FASDs last a lifetime. There is no cure for FASDs, but research shows that early intervention treatment services can improve a child’s development. 

There are many types of treatment options, including medication to help with some symptoms, behavior and education therapy, parent training, and other alternative approaches.  No one treatment is right for every child.
Good treatment plans will include close monitoring, follow-ups, and changes as needed along the way.
Also, “protective factors” can help reduce the effects of FASDs and help people with these conditions reach their full potential.

Protective factors include:
  • Diagnosis before 6 years of age
  • Loving, nurturing, and stable home environment during the school years
  • Absence of violence
  • Involvement in special education and social services




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Club Foot

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The Facts on Club Foot

Congenital talipes equinovarus, commonly known as club foot, is a foot deformity in which the foot is twisted inward with the toes pointing down. 

It affects approximately 1 in every 1,000 newborns in the US each year. It is more common in males. Club foot may affect one or both feet. In 30% to 50% of affected children, it involves both feet.

This condition sometimes runs in families. If one child in the family has club foot, the likelihood of another child having this condition increases to 10%.

Causes of Club Foot

The exact cause of club foot is not known. An abnormality of the tendons and ligaments in the foot causes an abnormal structure and position of the foot. In some children, bones may also be abnormal in terms of shape, size, or position. There may be a link to maternal smoking during pregnancy.
If the foot is abnormally positioned in the uterus during pregnancy, it may not grow into a normal shape, but this is not usually considered a "true" club foot.
Club foot may, in rare instances, be associated with spinal deformities such as spina bifida or other neuromuscular diseases; however, in these cases, the foot is usually more deformed.

Symptoms and Complications of Club Foot

Club foot is easy to recognize. The key identifying features are:
  • tightening of the Achilles tendon (heel cord)
  • inward turning of the front of the foot
  • downward-pointing toes
  • resting of the foot on its outer border
  • abnormal shape of the foot
  • rigidity and other changes in the movements of the foot
In some children, the foot may have a higher-than-normal arch. The foot and calf on the affected side are smaller than normal.
It is important to remember that although it is a painless condition at birth, club foot can worsen with time. If left untreated, the child may begin walking on the outer surface of the foot and the toes. This abnormal walking pattern causes hardening of the skin and development of corns and ulcers over the outer border of the foot. Wearing shoes is difficult, and over time it may become a crippling and unsightly condition.

Diagnosing Club Foot

Club foot is diagnosed at birth and may be diagnosed earlier, during pregnancy, or through ultrasound.
Although club foot may be diagnosed on the basis of physical examination alone, your doctor may also order X-rays of the foot in order to assess the position of the bones and to determine if there are any abnormalities in the bone. A complete physical examination is performed to rule out other spinal and muscular diseases.

Treating and Preventing Club Foot

The goal of treatment is to make a club foot functional, painless, and stable, especially for walking. A pediatric orthopedic surgeon experienced in this condition will normally be the best person to treat it. The earlier the treatment starts, the better the results.

Non-surgical treatment includes manipulating the foot into a corrected position and then holding it in position with a cast or splint with tapes. This is usually done 2 to 3 days after birth. The cast is applied from the toes to just above or below the knee and is changed every week until the infant is 3 to 6 months old. Your doctor will make regular assessments of this treatment. In most cases, it is apparent within 6 weeks whether the treatment is successful. An X-ray can also confirm this.
This treatment, if done by a trained doctor, is successful in about 50% of children with club foot. Special footwear or braces may be required to ensure that the muscles do not pull the foot back into the clubbed position. These may be used until the child is 2 or 3 years old.

Surgery may be performed to correct the abnormal tendons, ligaments, and joints. This may also include moving tendons into better positions for the best function. The surgery requires a hospital stay of 2 to 3 days. After surgery, a cast is applied to maintain the foot in the corrected position for 10 to 12 weeks. After the cast, a splint is used throughout the day. Once the child starts walking, the use of splint is gradually reduced.
There is no clear consensus regarding when to operate and which surgery to perform. Most orthopedic surgeons prefer to operate when the child is 6 months old, though some prefer to wait until 9 to 12 months of age.

If there are persistent bone abnormalities, surgery may be required when the child is older. An osteotomy (cutting the bone) can be performed when the child is at least 5 years old, or arthrodesis (fusing and stabilizing the bones) may be performed when the child is at least 10 years old. Not all children require more than one operation.

Physiotherapy is always an important part of the treatment. It may begin once the child is 3 months old. The therapist manipulates the affected foot and may also tape it. This alone may be successful in milder cases. Parents can learn these techniques and continue the treatment at home.
A chiropodist may need to be consulted for the treatment of corns and for custom insoles and shoes for the affected foot.

Most children do well with treatment when it is started early. If treatment is delayed, non-surgical treatment will not be effective and surgery will be more difficult and less successful. Some degree of deformity could persist. The foot and the calf on the affected side may remain smaller than normal.

Since the exact cause of club foot is not understood, there is no specific prevention. However, regular monitoring is recommended until the person reaches adulthood. Approximately 20% of affected children experience a recurrence of the club foot, usually in the first 2 to 3 years of life. The recurrence is more difficult to correct, and surgery is less successful in such cases. Your doctor may also advise using corrective shoes and splints until the child matures. But when treatment is started early, most children are able to enjoy full and active lives.



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