Congenital compression facies digital illustration

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ICD-10 code: Q67.1

Disease category: Q67: Congenital musculoskeletal deformities of head, face, spine and chest

Congenital Compression Facies: Understanding the Condition

Congenital compression facies is a rare condition that affects infants during their prenatal development. It is characterized by abnormal facial features, including a flattened nose, small chin, and a reduced vertical dimension of the face. This condition occurs due to external pressure on the developing fetus's face while in the womb.

Although the exact causes of congenital compression facies are not fully understood, it is believed to be the result of various factors. These may include the mother's body position, prolonged labor, uterine abnormalities, or the presence of multiple fetuses. However, it is important to note that this condition is not caused by any actions or behaviors of the mother during pregnancy.

During the prenatal period, the fetus's facial bones are still forming and are susceptible to external forces. When external pressure is applied to the face for an extended period, it can lead to the alteration of facial growth and development, resulting in congenital compression facies.

  1. Flattened Nose: One of the most noticeable features of congenital compression facies is a flattened nose. The nasal bridge appears lower than usual, and the nostrils may be wider or flatter in shape.
  2. Small Chin: Another characteristic of this condition is a small chin. The lower jaw may appear underdeveloped, leading to a receding chin.
  3. Reduced Vertical Dimension of the Face: Congenital compression facies can also affect the vertical dimension of the face. The distance between the forehead and the chin may be shorter than normal.

While congenital compression facies can affect an infant's facial appearance, it is essential to understand that it does not typically cause any functional problems or health issues. However, the psychological and social impacts on individuals with this condition may vary, and support from healthcare professionals and loved ones can be beneficial.

It is important for parents and caregivers to consult with a pediatrician or a specialist familiar with congenital compression facies for accurate diagnosis and appropriate guidance. Early intervention and management can help address any concerns and provide support for the affected child and their family.

In conclusion, congenital compression facies is a rare condition that affects the facial appearance of infants due to external pressure during prenatal development. Understanding the characteristics of this condition can help parents and caregivers seek appropriate medical advice and support for their child.

Treatment of Congenital compression facies:

Congenital Compression Facies: Exploring Treatment Options

Congenital compression facies is a condition that affects the development of an infant's facial structure, resulting in limited mobility and characteristic facial features. While the severity and specific symptoms vary from case to case, early intervention and appropriate treatment options are crucial for optimizing the chi...

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