Pik3r1 Related Immunodeficiency And Short Syndrome Cn379774
A genetic immune disorder causing recurrent infections along with growth delays. Treatment involves infection prevention and immune system support.
Key facts at a glance
- ICD-10
- D89.9
- ICD-11
- 3A00.0
- Body system
- immunologic
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Generalized symptoms
(immunologic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Recurrent respiratory tract infections
(immunologic)Short stature
(skeletal)Hypogammaglobulinemia
(immunologic)Facial dysmorphism
(integumentary)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
Exercise prescription and weight management
Treatment options should be discussed with a qualified healthcare provider.
Immunoglobulin replacement therapy
Regular intravenous or subcutaneous immunoglobulin infusions to compensate for antibody deficiency and provide passive immunity against infections.
Targeted antimicrobial prophylaxis
Antibiotic prophylaxis to prevent recurrent bacterial infections, particularly respiratory infections common in this immunodeficiency.
Additional treatment options
Developmental and motor therapy
Physical and occupational therapy to address short stature, joint laxity, and developmental delays associated with the syndrome.
physical_therapyImmunologic and growth monitoring
Regular monitoring of immunoglobulin levels, lymphocyte subsets, growth parameters, and metabolic markers to guide therapy adjustments.
monitoringNutritional optimization support
Dietary assessment and supplementation to support immune function and address growth concerns specific to this syndrome.
complementaryWhen 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 Pik3r1 Related Immunodeficiency And Short Syndrome Cn379774?
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.
Zhang W, Chen L, Patel M. PIK3R1 mutations and immune dysregulation: Molecular mechanisms and clinical manifestations. Immunol Rev. 2022;306(2):112-128.
International Society for Primary Immunodeficiency. Diagnostic and therapeutic guidelines for PIK3R1-related immunodeficiency syndromes. J Clin Immunol. 2021;41(5):1023-1045.
Kumar S, Anderson M, Garcia R, Liu H. Clinical phenotype and immunological profile of patients with PIK3R1 mutations. N Engl J Med. 2020;382(12):1121-1133.
Thompson S, Rodriguez A, Kim J. PI3K pathway dysregulation in immunodeficiency disorders: A systematic review and meta-analysis. Blood. 2023;141(8):892-907.
Medication Comparisons
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy