Other congenital malformations of upper limb(s), including shoulder girdle
ICD-10 Q74.0 is a billable code used to indicate a diagnosis of other congenital malformations of upper limb(s), including shoulder girdle.
Congenital malformations of the upper limbs, including the shoulder girdle, encompass a variety of structural abnormalities that can affect the bones, muscles, and soft tissues. These malformations may arise from genetic factors, environmental influences, or a combination of both. Common conditions include limb reduction defects, where one or more limbs are underdeveloped or absent, and deformities such as clubfoot or congenital hip dysplasia, which can affect limb function and mobility. Scoliosis, while primarily a spinal condition, can also be associated with upper limb malformations due to compensatory mechanisms. Accurate diagnosis often involves imaging studies and genetic testing to determine the underlying cause and to guide treatment options. Early intervention is crucial for optimizing functional outcomes and may include physical therapy, orthopedic interventions, or surgical correction. The complexity of these conditions necessitates a multidisciplinary approach, involving pediatricians, orthopedic surgeons, and geneticists to provide comprehensive care.
Detailed clinical notes describing the malformation, functional impact, and any associated conditions.
Assessment of a newborn with limb reduction defects or a child with clubfoot.
Consideration of developmental milestones and functional assessments in pediatric patients.
Genetic testing results, family history, and any syndromic associations.
Genetic counseling for families with a history of congenital limb malformations.
Understanding the genetic basis of malformations to guide treatment and family planning.
Used in conjunction with treatment for congenital malformations affecting joint function.
Document the indication for the procedure and any associated conditions.
Orthopedic specialists may require additional imaging documentation.
Documentation must include a detailed description of the malformation, any associated conditions, and the impact on function. Genetic testing results should also be included when applicable.
