(Q75) Other congenital malformations of skull and face bones

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176 216 in individuals diagnosis other congenital malformations of skull and face bones confirmed
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1 717 deaths with diagnosis other congenital malformations of skull and face bones
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1% mortality rate associated with the disease other congenital malformations of skull and face bones

Diagnosis other congenital malformations of skull and face bones is diagnosed Men are 37.25% more likely than Women

120 927

Men receive the diagnosis other congenital malformations of skull and face bones

821 (0.7 %)

Died from this diagnosis.

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55 289

Women receive the diagnosis other congenital malformations of skull and face bones

896 (1.6 %)

Died from this diagnosis.

Risk Group for the Disease other congenital malformations of skull and face bones - Men and Women aged 0

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In Men diagnosis is most often set at age 0-44, 55-64, 70-74
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Less common in men the disease occurs at Age 45-54, 65-69, 75-95+Less common in women the disease occurs at Age 40-59, 65-95+
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In Women diagnosis is most often set at age 0-39, 60-64

Disease Features other congenital malformations of skull and face bones

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Absence or low individual and public risk
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Other congenital malformations of skull and face bones - what does this mean

Other congenital malformations of skull and face bones occur when the normal development of the skull and face bones is disrupted during fetal development. this can result in abnormal growth and development of the skull and face bones, leading to deformities such as cleft lip and palate, craniosynostosis, and facial asymmetry.

What happens during the disease - other congenital malformations of skull and face bones

Other congenital malformations of skull and face bones is a condition in which the bones of the skull and face are abnormally developed during fetal development, leading to an abnormal facial appearance and skull shape. this is caused by a combination of genetic and environmental factors, including genetic mutations, maternal health during pregnancy, and environmental toxins. the exact cause of the malformation is usually unknown, but can be caused by a combination of genetic and environmental factors.

Clinical Pattern

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How does a doctor diagnose

  • Physical examination
  • X-ray
  • CT scan
  • MRI scan
  • Ultrasound scan
  • Genetic testing
  • Blood tests

Treatment and Medical Assistance

Main goal: To treat Other Congenital Malformations of Skull and Face Bones.
  • Evaluation of the malformation and the patient's medical history
  • Imaging tests to assess the extent of the malformation
  • Surgery to correct the malformation
  • Post-operative monitoring and follow-up
  • Medication to control pain and inflammation
  • Physical therapy to improve range of motion and strength
  • Counseling and support for the patient and family
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10 Days of Hospitalization Required
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Average Time for Outpatient Care Not Established

Other congenital malformations of skull and face bones - Prevention

The best way to prevent other congenital malformations of skull and face bones is to ensure that pregnant women receive adequate nutrition, prenatal care, and avoid exposure to environmental toxins. it is also important to seek genetic counseling prior to pregnancy if there is a family history of these malformations.

Specified forms of the disease

(Q75.0) Craniosynostosis
(Q75.1) Craniofacial dysostosis
(Q75.2) Hypertelorism
(Q75.3) Macrocephaly
(Q75.4) Mandibulofacial dysostosis
(Q75.5) Oculomandibular dysostosis
(Q75.8) Other specified congenital malformations of skull and face bones
(Q75.9) Congenital malformation of skull and face bones, unspecified