2025 ICD-10-CM code Q67.2
Dolichocephaly, a congenital condition characterized by an elongated head shape.
Medical necessity for intervention is determined by the severity of the dolichocephaly and the presence of any functional or cosmetic concerns.In mild cases, observation may be sufficient.In more severe cases, intervention may be necessary to address potential complications or improve head shape.
Diagnosis and management are typically overseen by pediatricians, geneticists, or craniofacial specialists.Assessment may involve physical examination, imaging studies (like skull x-rays or CT scans), and genetic testing to determine the underlying cause. Treatment depends on the severity and underlying cause and may range from observation to surgical intervention.
- Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- Q67 Congenital musculoskeletal deformities of head, face, spine and chest
In simple words: Dolichocephaly is a condition where a baby is born with a head that is longer than usual.
Dolichocephaly is a congenital skull deformity where the head is longer than typical, relative to its width.This results in a narrow and elongated head shape. It is present from birth.
Example 1: A newborn infant presents with a noticeably elongated head shape upon physical examination, diagnosed as dolichocephaly.No other abnormalities are detected, and the condition is attributed to positional molding in utero. Regular monitoring and repositioning techniques are recommended., A premature infant develops dolichocephaly due to prolonged time spent lying in the same position in the neonatal intensive care unit.Helmet therapy is initiated to help reshape the skull., A child is diagnosed with dolichocephaly as part of a genetic syndrome.Genetic counseling and further evaluation are recommended to assess for other associated conditions and develop a comprehensive management plan.
Documentation should include a detailed description of the head shape, including measurements (cephalic index).Any associated conditions or syndromes should be noted. Imaging results, genetic testing reports, and treatment plans should also be documented.
** Excludes1: sagittal craniosynostosis (Q75.01). This code is not used on the maternal record.
- Specialties:Pediatrics, Genetics, Craniofacial Surgery
- Place of Service:Office, Inpatient Hospital, Outpatient Hospital