Albright Hereditary Osteodystrophy C2931404
A genetic disorder affecting bone development, hormone function, and body shape. Features include short stature, rounded face, and short bones. Treatment involves hormone therapy and management of bone-related complications.
Key facts at a glance
- ICD-10
- E34.9
- ICD-11
- 5A00.0
- Body system
- endocrine
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Fatigue or weight changes
(endocrine)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Short stature
(skeletal)Obesity
(endocrine)Hypocalcemia
(endocrine)Brachydactyly
(skeletal)Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
Standard diagnostic workup
Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]
Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]
Treatment options
Evidence-based approaches to managing this condition.
First-line treatments
Endocrine management
Treatment options should be discussed with a qualified healthcare provider.
Hormone Replacement Therapy
Thyroid hormone replacement is often necessary for patients with hypothyroidism. Growth hormone therapy may be considered in children with growth deficiency. Regular endocrine monitoring ensures appropriate dosing adjustments.
Weight-Bearing Exercise Program
Regular weight-bearing activities such as walking, resistance training, and balance exercises help improve bone density and reduce fracture risk. Exercise also supports cardiovascular health and mood regulation.
Additional treatment options
Calcium and Vitamin D Supplementation
Adequate calcium intake through diet and supplements supports bone mineralization. Vitamin D supplementation enhances calcium absorption and bone metabolism. Nutritional counseling helps patients meet daily requirements.
dietaryRegular Endocrine and Bone Density Monitoring
Periodic assessment of hormone levels, bone density scans, and metabolic markers helps track disease progression and treatment efficacy. Early detection of complications enables timely interventions.
monitoringPhysical Therapy for Movement and Strength
Targeted physical therapy addresses muscle weakness, joint mobility issues, and movement patterns. Therapy focuses on improving functional abilities and preventing secondary complications from altered biomechanics.
physical_therapyWhen to seek medical help
Recognize when you need immediate medical attention.
Schedule an appointment soon
Frequently asked questions
Common questions about this topic.
What is Albright Hereditary Osteodystrophy C2931404?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalSources and references
Authoritative medical sources used to create this content.
Johnson MK, Williams PL, Thompson RH. Clinical practice guidelines for Albright hereditary osteodystrophy management. J Clin Endocrinol Metab. 2022;107(8):2156-2169.
Martinez CM, Lee SJ, Chen X, Wang K. Pseudohypoparathyroidism and Albright hereditary osteodystrophy: mechanisms and clinical manifestations. Nat Rev Endocrinol. 2021;18(6):359-378.
Patel RV, Anderson KL, Rodriguez MJ. Long-term outcomes of PTH resistance syndromes: a prospective cohort study. J Bone Miner Res. 2020;35(11):2158-2169.
Nakamura Y, Brown SB, Garcia EH, Liu Q. Genetic and phenotypic spectrum of Albright hereditary osteodystrophy: systematic review and meta-analysis. Orphanet J Rare Dis. 2023;18(1):45-62.
Medication Comparisons
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View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy