Laurence-Moon syndrome
ICD-10 Q87.84 is a billable code used to indicate a diagnosis of laurence-moon syndrome.
Laurence-Moon syndrome is a rare genetic disorder characterized by a combination of symptoms including retinitis pigmentosa, intellectual disability, obesity, hypogonadism, and polydactyly. It is classified as a syndromic form of obesity and is associated with various congenital malformations. The syndrome is caused by mutations in genes that are involved in the development and function of the central nervous system and other organ systems. Patients may present with additional congenital anomalies such as renal agenesis, skeletal deformities, and abnormalities of the skin and breast tissue. The condition is often diagnosed in childhood, and management typically involves a multidisciplinary approach to address the various health issues associated with the syndrome, including vision impairment, developmental delays, and metabolic concerns. Genetic counseling is recommended for affected families to understand the inheritance patterns and implications for future pregnancies.
Pediatric documentation must include growth parameters, developmental milestones, and specific congenital anomalies present.
Common scenarios include routine pediatric evaluations, referrals for developmental delays, and assessments for obesity-related complications.
Coders should ensure that all congenital anomalies are documented and linked to the primary diagnosis to avoid undercoding.
Genetic documentation should include family history, results of genetic testing, and any genetic counseling provided.
Scenarios include genetic counseling sessions, diagnostic evaluations for suspected syndromes, and follow-up assessments post-diagnosis.
Accurate coding requires understanding of genetic inheritance patterns and the implications of genetic findings on patient management.
Used during routine evaluations for developmental delays in children with Laurence-Moon syndrome.
Documentation must include the specific developmental concerns and results of the screening.
Pediatric specialists should ensure that developmental assessments are comprehensive and linked to the diagnosis.
Common congenital anomalies associated with Laurence-Moon syndrome include polydactyly, renal agenesis, and various skeletal deformities. Coders should ensure these are documented to provide a complete clinical picture.
