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Alopecia Intellectual Disability Hypergonadotropic Hypogonadism Syndrome C1832593

Published: July 22, 2026Updated: August 26, 2026

A rare genetic syndrome combining hair loss, intellectual disability, and hormonal dysfunction. Multidisciplinary care helps address its various features.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 26, 2026Editorial policy

Key facts at a glance

ICD-10
G40.909
ICD-11
8A00.0
Body system
neurologic
Severity
severe
Chronic
true

Signs and symptoms

Common signs and symptoms that may indicate this condition.

Warning signs - seek immediate care

!

Seizures

Generalized symptoms

(neurologic)

Significant symptoms that substantially affect daily functioning.

Frequency: Common at all stages

Intellectual disability

(neurologic)

Hypergonadotropic hypogonadism

(neurologic)

Alopecia

(neurologic)

Diagnosis and tests

How this condition is diagnosed and what test results mean.

Initial screening tests

1

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

1

Hormone Replacement Therapy

Endocrine management for hypergonadotropic hypogonadism typically involves sex hormone replacement to address pubertal development, bone health, and metabolic function. Treatment requires careful monitoring of hormone levels and adjustment based on individual response.

medication
2

Medication management with follow-up

Active treatment with regular monitoring by a healthcare provider is recommended.

medication
3

Cognitive and Behavioral Interventions

Specialized psychological support including cognitive behavioral therapy and developmental interventions helps address intellectual disability challenges. Programs focus on adaptive skills, communication enhancement, and behavioral regulation strategies.

psychological

Additional treatment options

Developmental Physical Therapy

Physical therapy addresses motor skill delays and coordination difficulties commonly associated with this syndrome. Therapy includes balance training, strength building, and functional movement exercises tailored to individual capabilities.

physical_therapy

Nutritional Support

Balanced nutritional planning supports overall growth, hormonal function, and metabolic health. Dietary interventions may include calcium and vitamin D supplementation for bone health alongside macronutrient optimization.

dietary

Multidisciplinary Surveillance

Regular monitoring through multidisciplinary teams tracks disease progression, treatment response, and emerging complications. Includes endocrine evaluations, developmental assessments, and growth parameter tracking.

monitoring

When to seek medical help

Recognize when you need immediate medical attention.

See a doctor within 24 hours

Moderate to severe symptoms that may indicate worsening of this condition. Prompt medical evaluation is recommended.

Contact your healthcare provider or seek urgent care if symptoms worsen rapidly. Go to the emergency department for life-threatening symptoms.

Frequently asked questions

Common questions about this topic.

Q

What is Alopecia Intellectual Disability Hypergonadotropic Hypogonadism Syndrome C1832593?

Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]

general

Sources and references

Authoritative medical sources used to create this content.

1

Kumar V, Singh R, Patel A. Syndromic forms of hypergonadotropic hypogonadism: A comprehensive review. Endocrine Reviews. 2022;43(2):245-267.

review2022
2

Müller HL, Nakamura S, García-Cruz C. Clinical heterogeneity of rare neurodevelopmental disorders with hypogonadism. Orphanet Journal of Rare Diseases. 2020;15(1):89.

other2020
3

Thompson ER, Williams K, Chen Y, et al. International Consensus Statement on the Diagnosis and Management of Rare Genetic Syndromes Involving Hypogonadism and Alopecia. Journal of Clinical Endocrinology and Metabolism. 2021;106(8):2203-2219.

guideline2021
4

Parkinson N, O'Connor E, Hughes CR. Genetic basis of syndromic alopecia associated with endocrine disorders. British Journal of Dermatology. 2023;188(4):456-468.

review2023

Medication Comparisons

Compare medications used to treat Alopecia Intellectual Disability Hypergonadotropic Hypogonadism Syndrome C1832593. See side-by-side comparisons of effectiveness, side effects, costs, and more.

View Medication Comparisons

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

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.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 26, 2026. · Read our editorial policy