Congenital morphological disturbances of hair, not elsewhere classified
ICD-10 Q84.1 is a billable code used to indicate a diagnosis of congenital morphological disturbances of hair, not elsewhere classified.
Congenital morphological disturbances of hair encompass a range of conditions characterized by abnormal hair growth patterns, texture, or distribution that are present at birth. These disturbances can manifest as hair loss, abnormal hair density, or unusual hair types, such as woolly hair or hair that is absent in certain areas. While some conditions may be isolated, others can be associated with broader syndromic presentations, including genetic syndromes that affect multiple systems. The etiology of these disturbances can be genetic, environmental, or a combination of both, and they may be linked to chromosomal abnormalities or other congenital malformations. Accurate diagnosis often requires a multidisciplinary approach, including dermatological evaluation and genetic testing, to determine the underlying cause and to guide management. Treatment options may vary based on the specific condition and its associated symptoms, ranging from cosmetic interventions to more complex medical management.
Pediatric documentation should include detailed growth and development assessments, family history, and any associated congenital anomalies.
Common scenarios include evaluation of infants with abnormal hair patterns, assessment of hair loss in children, and management of syndromic presentations.
Considerations include the age of onset, associated symptoms, and the potential impact on psychosocial development.
Genetic documentation needs to include results from chromosomal analysis, family pedigree, and any relevant genetic counseling notes.
Scenarios include genetic counseling for families with a history of congenital hair disorders and interpretation of genetic test results.
Considerations include understanding the inheritance patterns and implications for family members.
Used for follow-up visits in patients with congenital hair disorders.
Document the patient's history, examination findings, and any treatment plans.
Pediatricians should focus on growth and development assessments.
Common congenital hair disorders include conditions like woolly hair syndrome, hypotrichosis, and other syndromic presentations that may involve hair morphology. Accurate coding requires understanding the specific condition and its implications.
