2025 ICD-10-CM code Q79.6
(Valid) Effective Date: N/A Revision Date: N/A Congenital malformations, deformations and chromosomal abnormalities - Ehlers-Danlos syndromes 17 Feed
This code encompasses a group of heritable connective tissue disorders, known as Ehlers-Danlos syndromes (EDS). EDS is primarily characterized by joint hypermobility, skin hyperextensibility, and tissue fragility.
Medical necessity for services related to EDS depends on the specific manifestations and severity of the condition.It may include genetic testing for diagnosis, physical therapy for joint stabilization, pain management, and other interventions as needed.
Diagnosis and management of Ehlers-Danlos syndromes typically involve a multidisciplinary approach, often including geneticists, dermatologists, orthopedists, cardiologists, and physical therapists. Clinical responsibility includes accurate diagnosis based on clinical findings, genetic testing, and family history, as well as developing a comprehensive management plan to address the specific needs of the individual.
In simple words: Ehlers-Danlos syndrome (EDS) is a group of disorders that affect connective tissues supporting the skin, joints, blood vessels, and other organs.People with EDS often have overly flexible joints, stretchy skin, and fragile tissues that bruise or scar easily. There are many different types of EDS, ranging from mild to severe.
Ehlers-Danlos syndromes represent a clinically and genetically heterogeneous group of heritable connective tissue disorders.They are generally characterized by joint hypermobility (the ability of joints to move beyond their normal range), skin hyperextensibility (the skin's ability to stretch beyond its normal limits), and tissue fragility.These manifestations result from defects in the structure, production, or processing of collagen and other connective tissue proteins.
Example 1: A 25-year-old individual presents with chronic joint pain, frequent dislocations, and velvety, hyperextensible skin. After a thorough evaluation, including genetic testing, they are diagnosed with Hypermobile EDS (hEDS)., A child is brought to the pediatrician with recurrent joint subluxations, easy bruising, and delayed wound healing.Genetic testing confirms a diagnosis of Classical EDS (cEDS)., A pregnant woman with a family history of Vascular EDS (vEDS) undergoes genetic counseling and testing to assess her risk of passing on the condition and plan for potential complications during pregnancy and delivery.
Documentation for EDS should include detailed family history, physical exam findings (including Beighton score for joint hypermobility), skin assessment, and results of any genetic testing or imaging studies.Specific documentation requirements will vary based on the type of EDS suspected.
** Excludes2: congenital (sternomastoid) torticollis (Q68.0)
- Specialties:Genetics, Dermatology, Orthopedics, Cardiology, Physical Therapy, Rheumatology
- Place of Service:Office, Inpatient Hospital, Outpatient Hospital, Specialist Clinic