Monosomy X C0242526
A chromosomal condition in females where one X chromosome is partially or completely missing. It can affect growth, development, and puberty. Treatment addresses individual symptoms and may include hormone therapy.
Key facts at a glance
- ICD-10
- Q89.9
- ICD-11
- LA00.0
- Body system
- congenital
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Generalized symptoms
(congenital)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
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
Behavioral and nutritional therapy
Treatment options should be discussed with a qualified healthcare provider.
Hormone Replacement Therapy
Estrogen replacement therapy to induce puberty, maintain bone health, and support cardiovascular function. Typically initiated in early adolescence under specialist supervision.
Comprehensive Multisystem Monitoring
Regular cardiac monitoring including echocardiograms, renal ultrasound, hearing assessments, and endocrine evaluations to detect and manage associated conditions.
Additional treatment options
Cardiac Anomaly Correction
Surgical intervention for structural cardiac abnormalities such as bicuspid aortic valve or coarctation of the aorta when clinically indicated.
surgicalMusculoskeletal Intervention
Physical therapy programs addressing lymphedema, hypotonia, and skeletal abnormalities including scoliosis and pes planus commonly seen in this population.
physical_therapyPsychological and Developmental Support
Psychological counseling and developmental support addressing social challenges, self-esteem, body image concerns, and infertility-related emotional impact.
psychologicalWhen 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 Monosomy X C0242526?
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.
Gravholt CH, Viuff MH, Brun S, et al. Clinical Practice Guidelines for the Care of Girls and Women with Turner Syndrome. Eur J Endocrinol. 2022.
Bondy CA. Cardiovascular Anomalies in Turner Syndrome. J Endocrinol Invest. 2021.
Davenport ML, Nickel RE, Kuntze J, et al. Growth Hormone Treatment in Girls with Turner Syndrome: Long-term Outcomes. Horm Res Paediatr. 2020.
Bintang AK, Wibowo T, Harzif AK, et al. Pregnancy Outcomes in Turner Syndrome: A Systematic Review and Meta-Analysis. Int J Womens Health. 2023.
Medication Comparisons
Compare medications used to treat Monosomy X C0242526. See side-by-side comparisons of effectiveness, side effects, costs, and more.
View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy