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TALIPES

By : Madam Rohimah bt Ismail

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LEARNING OUTCOME
1. State the definition of talipes
2. State the etiology of talipes
3. State the type factor for talipes
4. State the clinical manifestation of talipes
5. State the diagnostic for talipes
6. State the treatment of talipes

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INTRODUCTION

Talipes is a deformity of the foot and ankle that a child can be born
with this problem.

The term “talipes” was coined by Little in 1839. He derived it from


the Latin “Talus”(ankles) and pes( foot)

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DEFINITION

• Clubfoot is a complex deformity


of foot result of complicated
interrelationship between
bone, ligaments and muscles.

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CONT ..

• It occurs in one out of 1000 live


birth.
• Boys affected twice more than
girls

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ETIOLOGY

• Hereditary-defective gene
• Excessive pressure of amniotic fluid on
fetus causes excessive pressure of uterine
wall on fetus.
• Mechanical cause(Uterine compression)
• Arrested fetal development
• Circulatory failure to calf and foot muscles
• Irradiation(maternal) during pregnancy.

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CLASIFICATION

1. Talipes Equinovarus:
• 95% all cases.
• The foot is fixed in plantar flexion
and deviates medially that is the
heal is elevated.
• The child walks on the toes and the
outer boarder of the foot.

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CONT ..
Talipes Calcaneovalgus:

• In this the foot is dorsiflexed and


deviates laterally that is the heel is
turned outward from the midline of
the body and the anterior part of
the foot is elevated on the outer
border.

• If not corrected the child walks on


the outwardly turned heel and the
inner border of the foot.

• These conditions may be unilateral


or bilateral ALPINE SKI HOUSE 8
• 3. Talipes varus:
• The heel’s being turned inward from the
midline of the leg.
• Only the outer portion of the sole rests on
the floor

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4.Talipes valgus:
• Due to the heels being turned
outward from the midline of the leg.
• Only the inner side of the sole rests
on the floor

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5. Talipes Equinovalgus:
• Due to the heels being elevated and turned
outward from the midline of the body.
6. Talipes calcaneovarus:
• Due to the heels being turned towards the
midline of the body and anterior part of the
foot being elevated .
• Only the heels rests on the floor.

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CLINICAL
MANIFESTATION

Usually, clubfoot is painless in children.

• Discomfort and become a noticeable disability.

• The foot will remain twisted out of shape and the


affected leg, may be shorter and smaller than the
other.

• Poor child growth and development.

• Body image disturbance

• The calf muscles are generally underdeveloped

• Stiff rigid, foot of varying degrees.


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DIAGNOSTIC
EVALUATION
• History collection

• Physical examination

• Ultrasound scanning during pregnancy

• X-rays

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MANAGEMENT

Non operative management:


• Two categories of clubfoot are identified.
• 1. Easy or correctable clubfoot: which is
corrected with manipulation , casting and
splintage alone.
• 2. Resistant clubfoot: It is that which
responds poorly to splintage and
manipulative treatment. It requires
operative management

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• Ponseti method is popular manipulation
method to correct clubfoot.

• This is not painful or uncomfortable for the


child.

• The surgeon will do gentle movements and


stretches with the baby's foot before each
cast is put on. These help slowly move the
foot toward its correct position. Then, the
cast is put on to hold that new position until
it's time for the next cast

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Surgical management

• In children younger than 5 years , correction


can be achieved with soft tissue procedure.

• Children older than 5years require bone


reshaping eg. Dorselateral wedge excision of
the calcaneocuboid joint or osteotomy of
the calcaneum to correct varus.

• Lateral wedge torsectomy or triple fusion is


required if the child is older than 10 years.

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NURSING DIAGNOSIS

• Impaired skin integrity related to application of casts

• Parental anxiety related to club foot

• High risk for body image disturbance related to


deformity of club foot

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MUSCULAR
DISTROPHY

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LEARNING
OUTCOME
• State the definition of MD

• State the causes of MD

• State the risk factor for MD

• State the symptom of MD

• State the complication of MD

• State the diagnostic for MD

• State the treatment of MD

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DEFINITION
Muscular dystrophy (MD) is a genetic disorder
that gradually weakens the body's muscles.

It's caused by incorrect or missing genetic


information that prevents the body from
making the proteins needed to build and
maintain healthy muscles.

A child who is diagnosed with MD gradually


loses the ability to do things like walk, sit
upright, breathe easily, and move the arms and
hands.

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TYPE OF MD

Major types:

• Duchenne and Becker,

• Emery-Dreifuss

• Limb-girdle,

• Oculopharyngeal,

• Facioscapulohumeral,

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CONT ..

• Can occur at any age


• Most common in young males.
• Type is based on what age the individual is when muscular dystrophy appears
• Also depends on how severe the disease is, which muscles it affects, rate of
progression.
• Some types of muscular dystrophy only affect males.
• Some individuals with this disease experience mild symptoms, while others suffer
from severe muscle weakness, dying at an early age.

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CAUSES
Certain genes are involved in making proteins
that protect muscle fibers. Muscular dystrophy
occurs when one of these genes is defective.

Each form of muscular dystrophy is caused by a


genetic mutation particular to that type of the
disease. Most of these mutations are inherited.

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RISK FACTOR

• Muscular dystrophy occurs in both


sexes and in all ages and races.
• However, the most common variety,
Duchenne, usually occurs in young
boys.
• People with a family history of
muscular dystrophy are at higher risk
of developing the disease or passing
it on to their children.

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SYMPTOM
Muscle weakness.

Myotonic: muscle spasms or stiffening


after use, hand weakness, foot drop

Clumsiness, frequent falling, difficulty


getting up, waddling gait, curvature of
the spine.

Drooling, eyelid drooping

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COMPLICATION

• Trouble walking. The child with muscular dystrophy eventually need to use a wheelchair.

• Trouble using arms. Daily activities can become more difficult if the muscles of the arms and shoulders are affected.

• Shortening of muscles or tendons around joints (contractures). Contractures can further limit mobility.

• Breathing problems. Progressive weakness can affect the muscles associated with breathing. The child with MD might
eventually need to use a breathing assistance device (ventilator), initially at night but possibly also during the day.

• Curved spine (scoliosis). Weakened muscles might be unable to hold the spine straight.

• Heart problems. Muscular dystrophy can reduce the efficiency of the heart muscle.

• Swallowing problems. If the muscles involved with swallowing are affected, nutritional problems and aspiration pneumonia
can develop. Feeding tubes might be an option.

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Muscle biopsy

DIAGNOSTIC
DNA testing

Blood enzyme tests

Electromyography or nerve conduction


tests

Electrodes are used to test the muscle


and/or nerves

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TREATMENT

• No cure

• Medications and therapy can relieve symptoms and


slow progression of the disease

• However, scientists are researching ways to insert a


working dystrophin gene into muscles of boys with
Duchenne and Becker MD

• Also, researchers are exploring potential muscle-


building drugs to help reverse progression

• Dietary supplements, creatine, and glutamine are other


potential treatments being studied

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CONT…

• Braces, wheelchairs, and canes can improve mobility

• Surgery on the spine or legs also may be an option to


improve function.

• Exercise! People suffering from MD should be as active


as possible. Primary focus is on gaining muscular
strength and endurance

• Physical inactivity may make the disease worse

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MEDICATION
Corticosteroids can slow muscle damage in
patients with Duchenne muscular dystrophy.

Phenytoin, procainamide, or quinine may treat


delayed muscle relaxation for those with
Myotonic MD.

Medications can also be prescribed to treat


heart problems in some forms of muscular
dystrophy

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