Congenital shortening of upper limb
ICD-10 Q71.81 is a billable code used to indicate a diagnosis of congenital shortening of upper limb.
Congenital shortening of the upper limb refers to a condition where one or both arms are shorter than normal due to developmental anomalies during fetal growth. This condition can result from various factors, including genetic syndromes, environmental influences, or isolated limb reduction defects. The shortening may affect the humerus, radius, or ulna, leading to functional limitations and aesthetic concerns. Associated congenital malformations may include syndactyly, polydactyly, or other limb deformities. The condition can be diagnosed through physical examination and imaging studies, such as X-rays, to assess the degree of shortening and any associated skeletal anomalies. Treatment often involves a multidisciplinary approach, including orthopedic interventions, physical therapy, and, in some cases, surgical correction to improve function and appearance. Early intervention is crucial for optimizing developmental outcomes in affected children.
Detailed growth and development assessments, including limb measurements and functional evaluations.
Assessment of a newborn with suspected limb shortening, follow-up evaluations for developmental milestones.
Consideration of family history and potential genetic syndromes associated with limb malformations.
Genetic testing results, family pedigree, and documentation of any syndromic associations.
Genetic counseling for families with a history of congenital limb defects, evaluation of syndromic conditions.
Understanding the genetic basis of limb malformations and implications for family planning.
Used in conjunction with limb shortening for joint evaluation.
Document the joint involved and reason for aspiration.
Orthopedic specialists may require additional imaging documentation.
Documentation must include detailed measurements of the limb, any associated congenital anomalies, and a clear treatment plan. Ensure that all clinical findings are recorded to support the diagnosis.
