Cleft lip-Cleft Palate

Subject: Midwifery III (Theory)

Overview

The lip develops between the fourth and seventh weeks of pregnancy. During pregnancy, body tissue and special cells from each side of the head grow toward the center of the face and join together to form the face. This fusion of tissue gives rise to facial features such as the lips and mouth. A cleft lip can occur on one or both sides of the lip, or it can occur in the middle of the lip, which is very rare. Children who have a cleft lip and palate may also have a cleft palate. The causes of orofacial clefts in most infants are unknown. Because of genetic changes, some children have cleft lip or cleft palate. Cleft lip and palate are thought to be the result of a genetic defect.

Cleft lip and palate are birth defects that actually happen when a baby's lip or mouth do not develop properly during pregnancy. These birth defects are usually referred to as "orofacial clefts."

Cleft lip: Between the fourth and seventh weeks of pregnancy, the lip develops. Body tissue and special cells from each side of the head grow toward the center of the face and join together to form the face as a baby develops during pregnancy. This fusion of tissue results in the formation of facial features such as the lips and mouth. A cleft lip occurs when the tissue that makes up the lip does not completely join before birth. As a result, an opening appears in the upper lip. The lip opening can be a small slit or a large opening that extends through the lip and into the nose. A cleft lip can occur on one or both sides of the lip, or it can occur in the middle of the lip, which is extremely rare. Children who have a cleft lip may also have a cleft palate.

Cleft palate: Between the sixth and ninth weeks of pregnancy, the palate (the roof of the mouth) develops. A cleft palate occurs when the tissue that makes up the roof of the mouth does not completely fuse together during pregnancy. Both the front and back parts of the palate are open in some babies. Only a portion of the palate is open in other babies.

Causes:

Most infants' orofacial clefts are caused by unknown factors. Some children have cleft lip or cleft palate due to genetic changes. Cleft lip and palate are thought to be caused by a combination of genes and environmental factors, such as what the mother comes into contact with in her environment, what she eats or drinks, and certain medications she uses during pregnancy.

Risk factors:

  • Smoking: Women who smoke during their pregnancy are more likely than women who do not smoke to have a baby with an orofacial cleft.
  • Diabetes: Women who have diabetes before pregnancy have a higher risk of having a child with cleft lip and palate, compared to women who do not have diabetes.
  • Use of certain medicine: Women who took certain epilepsy medications, such as topiramate or valproic acid, during the first trimester (the first three months) of pregnancy have an increased risk of having a baby with cleft lip and/or cleft palate, compared to women who did not take these medications.

Signs and symptoms:

A split (cleft) in the lip or palate is usually noticeable at birth. Cleft lip and palate can express as:

  • A split in the lip and roof of the mouth (palate) can occur on one or both sides of the face.
  • A split in the lip that can be as small as a notch or can extend from the lip through the upper gum and palate into the bottom of the nose.
  • A split in the roof of the mouth that has no effect on the face's appearance.

A cleft occurs less frequently in the muscles of the soft palate (sub-mucous cleft palate), which are located at the back of the mouth and are covered by the mouth's lining. This type of cleft often goes unnoticed at birth and may not be diagnosed until symptoms appear later. Submucous cleft palate signs and symptoms may include:

  • Feeding difficulties
  • Difficulty swallowing, with the possibility of liquids or foods coming out the nose
  • Voice of Nasal Speaking
  • Ear infections that are chronic

Diagnosis:

  • A routine ultrasound can detect orofacial clefts, particularly cleft lips with or without cleft palate, during pregnancy.
  • Certain types of cleft palate, such as the submucous cleft palate and bifid uvula, may not be diagnosed until later in life.

Treatment:

  • When a child is about 3-6 months old, he or she can have a cleft lip repaired.
  • Unilateral cleft lip repair can take 3-6 weeks.
  • A 4.5kg infant with a hemoglobin of 11.8 gm/dl and no respiratory infection is a candidate for surgery.
  • Cleft palate surgery is usually performed before the child learns to speak.

Nursing management of cleft lip and cleft palate:

  • By displaying another baby with the same condition, the mother can be reassured and relieved of her distress.
  • Feeding should be done slowly and in an upright position. Sucking breast is not hampered by a cleft lift lip in the absence of a cleft palate. In severe cases of cleft lip and palate, a nipple must be spoon-fed from birth. To maintain lactation, breast milk should be expressed while breastfeeding.
  • Cleft palates tend to swallow a lot of air while feeding, so wind must be brought in.
  • After feeding, rinse the mouth with water.
Things to remember
  • Between the fourth and seventh weeks of pregnancy, the lip develops.
  • Body tissue and special cells from each side of the head grow toward the center of the face and join together to form the face as a baby develops during pregnancy.
  • This fusion of tissue results in the formation of facial features such as the lips and mouth.
  • A cleft lip can occur on one or both sides of the lip, or it can occur in the middle of the lip, which is extremely rare.
  • Children who have a cleft lip may also have a cleft palate.
  • Most infants' orofacial clefts are caused by unknown factors.
  • Some children have cleft lip or cleft palate due to genetic changes.
  • Cleft lip and palate are thought to be caused by a combination of genes and environmental factors, such as what the mother comes into contact with in her environment, what she eats or drinks, and certain medications she uses during pregnancy. A split (cleft) in the lip or palate is usually noticeable at birth.
  • A cleft occurs less frequently in the muscles of the soft palate (sub-mucous cleft palate), which are located at the back of the mouth and are covered by the mouth's lining.
  • This type of cleft often goes unnoticed at birth and may not be diagnosed until symptoms appear later.
  • The only treatment is surgical correction.
Questions and Answers

Between the fourth and seventh weeks of pregnancy, the lip develops. Body tissue and unique cells from each side of the head grow toward the middle of the face during pregnancy and come together to form the face. The lips and mouth are formed by the tissue coming together. If the tissue that forms the lip does not completely unite before birth, a cleft lip results. The upper lip becomes open as a result of this.

Most newborns with orofacial clefts have unknown reasons. Some kids are born with cleft lips or palates due to genetic abnormalities. The causes of cleft lip and cleft palate are thought to be a result of a genetic predisposition as well as environmental exposure, dietary habits, and medications taken by the mother during pregnancy, among other things.

Risk Factors:

  • Smoking
    • Compared to pregnant women who do not smoke, pregnant women who smoke have a higher risk of having a baby with an orofacial cleft.
  • Diabetes
    • Compared to women who did not have diabetes, those who were diagnosed with it prior to conception have a higher risk of giving birth to a child who has a cleft lip or palate.
  • Use of Certain Medicines
    • Compared to women who didn't take these medications, women who used topiramate or valproic acid throughout the first trimester (the first 3 months of pregnancy) doubled their risk of having a baby with cleft lip with or without cleft palate.

A split (cleft) in the lip or palate is typically obvious from birth. The symptoms of cleft lip and palate include:

  • One or both sides of the face may be affected by a split in the lip and palate (roof of the mouth).
  • A break in the lip that may only be visible as a minor notch or may extend through the upper gum and palate and into the bottom of the nose
  • A gap in the roof of the mouth that has no impact on facial appearance

Less frequently, a cleft only affects the soft palate muscles (sub-mucous cleft palate), which are in the back of the mouth and protected by the lining of the mouth. This kind of cleft is frequently undetected at birth and may not be identified until later when symptoms manifest. Submucous cleft palate symptoms and signs can include:

  • Having trouble eating
  • Swallowing issues that could cause food or fluids to leak out of the nose
  • Speaking with a nasal tone
  • Persistent ear infections

Surgery is the only form of treatment.

  • When the child is between three and six months old, the cleft lip may be fixed.
  • Repairs for unilateral cleft lips might take three to six weeks.
  • Surgery is an option for infants weighing 4.5 kg with hemoglobin levels of 11.8 g/dl and no respiratory infections.
  • Surgery for a cleft palate is typically performed before the kid learns to speak.

Nursing care for people with cleft lip and palate:

  • By displaying a baby with the same problem, the mother must be reassured and her distress soothed.
  • Feeding should be done gently and standing up. Breast sucking is unaffected by cleft raise lip without cleft palate. severe cleft lip and palate instances necessitate breast and spoon feeding from birth. To maintain lactation while breastfeeding, breast milk should be expressed.
  • When feeding, people with cleft palates frequently ingest a lot of air, thus it's important to remove it.
  • Give water to wipe the mouth after feeding.

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