Q71: ICD10 Code for Reduction defects of upper limb

Q71 is the ICD10 code used for documenting Reduction defects of upper limb involving congenital bone or musculoskeletal abnormalities.

Q71 - Reduction defects of upper limb

Q71 documents Reduction defects of upper limb, which encompasses a range of congenital anomalies affecting bones, limbs, joints, and overall musculoskeletal development visible at birth or early childhood.

Symptoms

  • Hip dislocation – Related to congenital hip deformities (Q65)
  • Clubfoot or flatfoot – Seen in congenital foot deformities (Q66)
  • Extra fingers or toes – Known as polydactyly (Q69)
  • Fused digits – Syndactyly (Q70)
  • Shortened or missing limbs – Related to reduction defects (Q71–Q73)

Diagnosis

Diagnosis typically involves physical examination at birth, X-rays, MRI imaging for complex deformities, and sometimes genetic studies to detect associated syndromes affecting the musculoskeletal system.

ICD10 Code Usage

ICD10 code Q71 is used in EHRs, orthopedic surgical planning, early intervention services, physical therapy programs, and insurance claims for congenital musculoskeletal disorders.

Related Codes

FAQs

Q1: What is ICD10 code Q71?
A: It is used to document Reduction defects of upper limb involving congenital skeletal and muscular deformities.

Q2: Are all musculoskeletal deformities surgically corrected?
A: Not always; some minor deformities may be managed with therapy or observation, while others need surgery.

Q3: Can these deformities be detected before birth?
A: Severe limb or skeletal malformations may be suspected on prenatal ultrasound.

Q4: What is the prognosis for congenital limb defects?
A: With modern surgical and prosthetic interventions, outcomes are often excellent, depending on severity.

Q5: What causes osteochondrodysplasias?
A: These are often genetic disorders affecting bone growth and development (Q77–Q78).

Conclusion

ICD10 code Q71 ensures standardized documentation of Reduction defects of upper limb, allowing early diagnosis, management planning, and optimal functional outcomes for individuals with congenital musculoskeletal anomalies.

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