basal ganglia calcification, idiopathic, childhood-onset | Kisho | Kisho

basal ganglia calcification, idiopathic, childhood-onset

Rare Disease

MONDO:0007247

Also known as:

basal ganglia calcification, idiopathic, childhood-onsetIBGC childhood onsetIBGC, childhood-onset

Genes

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Clinical Trials

1 active

Newborn Screening

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Patient Groups

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Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

How we create this content →

Feb 7, 2026

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Clinical Trials

Research studies investigating treatments and therapies for this condition.

Active Trials

Total Trials

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Data from ClinicalTrials.gov Jan 7, 2026

Clinical Trials

Research studies investigating treatments and therapies for this condition.

Active Trials

Total Trials

Filter trials on ClinicalTrials.gov:

View Recruiting Trials View All Trials

Data from ClinicalTrials.gov Jan 7, 2026

Overview

Basal ganglia calcification, idiopathic, childhood-onset is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Symptoms & Signs

The condition is also known by several synonyms, including bilateral striopallidodentate calcinosis childhood-onset and cerebral calcification nonarteriosclerotic idiopathic childhood-onset. Currently, there are no known associated genes, inheritance patterns, or documented symptoms. Additionally, there are no orphan drugs under investigation for this condition.

Prognosis & Outlook

Patients and caregivers are encouraged to seek consultation with specialists familiar with basal ganglia disorders. Genetic counseling may be beneficial, especially if there is a concern about hereditary aspects. Connecting with rare disease registries and online patient communities can provide additional support and resources.

Quick Resources

Helpful links for rare disease information and support

GARD (Genetic and Rare Diseases Information Center)NORD (National Organization for Rare Disorders)

General Questions to Consider

Questions that may be helpful when speaking with your healthcare team

•Are there specialists or centers of excellence with experience in this condition?
•Is there a patient registry I could participate in?
•What clinical trials might be available for this condition?
•Are there patient advocacy groups I should connect with?

Clinical

Limited Clinical Data

Clinical profile data for this condition is not yet available. Phenotype information may still be loading below.

Treatment

Clinical Trials

Research studies investigating treatments and therapies for this condition.

Active Trials

Total Trials

Filter trials on ClinicalTrials.gov:

View Recruiting Trials View All Trials

Data from ClinicalTrials.gov Jan 7, 2026

Support

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:114100

GARD

Genetic and Rare Diseases Info Center

GARD:9598

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AI-Generated Content: This summary was generated using AI. Always consult with qualified healthcare providers for medical guidance.

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basal ganglia calcification, idiopathic, childhood-onset

Patient-Friendly Information

Clinical Trials

Clinical Trials

Overview

Overview

Symptoms & Signs

Prognosis & Outlook

Quick Resources

General Questions to Consider

Clinical

Limited Clinical Data

Treatment

Clinical Trials

Support

External Resources

OMIM

GARD

Related Diseases

Know a Patient Advocacy Group for this condition?

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