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immunodeficiency 7
ICD-10 Codes
Related ICD-10:
Description
Signs and Symptoms
Common Signs and Symptoms of Immunodeficiency
Immunodeficiency disorders can manifest in various ways, making it essential to recognize the signs and symptoms early on. Here are some common indicators:
- Recurrent Infections: People with immunodeficiency often experience repeated infections, such as:
- Ear infections (otitis media) [1][2]
- Sinus infections (sinusitis) [3][4]
- Pneumonia [5][6]
- Bronchitis [7]
- Meningitis [8]
- Inflammation and Infections: Immunodeficiency can lead to inflammation and infection of internal organs, such as the spleen, liver, or lymph nodes [9][10].
- Fatigue and Weight Loss: Feeling extremely tired, like when you have the flu, could be a sign of immunodeficiency [11]. Additionally, people with this condition may experience weight loss due to chronic infections.
- Chronic Diarrhea: Some individuals with immunodeficiency may experience chronic diarrhea, which can lead to dehydration and electrolyte imbalances [12].
- Family History: A family history of primary immunodeficiency can also be an indicator of the condition [13].
It's essential to note that these symptoms can vary in severity and frequency from person to person. If you or someone you know is experiencing any of these signs, it's crucial to consult a healthcare professional for proper diagnosis and treatment.
References: [1] Context 3 [2] Context 5 [3] Context 4 [4] Context 8 [5] Context 6 [6] Context 9 [7] Context 10 [8] Context 11 [9] Context 7 [10] Context 12 [11] Context 13 [12] Context 14
Additional Symptoms
- Recurrent Infections
- Family History
- Chronic Diarrhea
- Fatigue and Weight Loss
- Inflammation and Infections of internal organs (spleen, liver, or lymph nodes)
Diagnostic Tests
Diagnostic Tests for Immunodeficiency
Immunodeficiency disorders can be diagnosed through various laboratory tests, which help identify the underlying cause and type of disorder. According to [7], one of the best screening tests for defects in the classical complement pathway is the total hemolytic complement activity (CH50) assay.
- Complement levels: Blood tests can measure complement levels, which are essential for fighting infections.
- Total hemolytic complement activity (CH50): This test screens for defects in the classical complement pathway.
- Antibody titers: Measuring antibody levels can help diagnose immunodeficiency disorders.
These diagnostic tests are crucial in confirming a diagnosis of immunodeficiency and identifying the type of disorder. They often involve blood tests, including complete blood counts (CBCs), to detect abnormalities in blood cells characteristic of specific immunodeficiency disorders [12].
Additional Tests
Depending on the clinical findings or initial test results, additional tests may be indicated for confirmation. These can include:
- Specific and advanced laboratory tests: These tests are used to confirm a diagnosis of immunodeficiency and identify the type of disorder.
- Immunoglobulins blood test: This test measures the levels of certain antibodies in the blood.
These diagnostic tests help healthcare providers determine the best course of treatment for individuals with immunodeficiency disorders.
Additional Diagnostic Tests
- Antibody titers
- Immunoglobulins blood test
- Complement levels
- Total hemolytic complement activity (CH50)
- Specific and advanced laboratory tests
Treatment
Treatment Options for Immunodeficiency
According to search result [7], the treatments most used for recurrent infections that occur in primary and secondary immunodeficiency are:
- Antibiotics
- Anti-fungals
- In some cases, other medications such as corticosteroids or immunosuppressive agents may be prescribed.
These treatments aim to manage symptoms and prevent complications associated with immunodeficiency. However, it's essential to note that individual risks and benefits should be discussed with a healthcare provider, as mentioned in search result [4].
Additional Treatment Options
Search results [2] and [5] also mention other treatment options for primary immunodeficiency, including:
- Gene therapy: This involves using the person's own stem cells to correct the genetic defect causing the immunodeficiency.
- Stem cell transplantation: This involves replacing the person's immune system with a healthy one from a donor.
These treatments are still being researched and developed, but they offer promising alternatives for individuals with primary immunodeficiency.
Recommended Medications
- Corticosteroids
- Immunosuppressive agents
- Antibiotics
- Gene therapy
- Stem cell transplantation
- Anti-fungals
💊 Drug information is sourced from ChEBI (Chemical Entities of Biological Interest) database. Always consult with a healthcare professional before starting any medication. Click on any medication name for detailed information.
Differential Diagnosis
Differential Diagnoses for Immunodeficiency
Immunodeficiency can be caused by various factors, and it's essential to consider differential diagnoses when evaluating a patient with suspected immunodeficiency. Here are some conditions that may present similarly to immunodeficiency:
- Agammaglobulinemia: A rare genetic disorder characterized by the absence or low levels of all classes of immunoglobulins (IgG, IgA, and IgM).
- Atopic Dermatitis: An inflammatory skin condition that can be associated with immunodeficiency in some cases.
- Cartilage-Hair Hypoplasia: A rare genetic disorder characterized by short stature, sparse hair, and recurrent infections, which may mimic immunodeficiency symptoms.
- Complement Deficiencies: Conditions where the complement system is impaired, leading to increased susceptibility to infections.
- Congenital TORCH (Toxoplasma, Rubella, Cytomegalovirus, Herpes simplex) Infections: A group of congenital infections that can cause immunodeficiency-like symptoms.
These conditions should be considered in the differential diagnosis of immunodeficiency, especially when evaluating patients with recurrent infections or other immune-related symptoms. [7][8]
Additional Information
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- https://w3id.org/def/predibionto#has_symptom_6486
- owl#annotatedSource
- t383676
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- DOID:0111977
- oboInOwl#hasDbXref
- UMLS_CUI:C3809332
- oboInOwl#hasExactSynonym
- TCR-alpha-beta-positive T-cell deficiency
- rdf-schema#label
- immunodeficiency 7
- IAO_0000115
- A T cell deficiency characterized by decreased or absent CD3+ T cells with TCR-alpha/beta expression, immune dysregulation, recurrent infections, and failure to thrive that has_material_basis_in homozygous or compound heterozygous mutation in the TRAC gene on chromosome 14q11.2.
- rdf-schema#subClassOf
- t384197
- oboInOwl#inSubset
- http://purl.obolibrary.org/obo/doid#DO_rare_slim
- IDO_0000664
- http://purl.obolibrary.org/obo/GENO_0000148
- relatedICD
- http://example.org/icd10/D84.9
- 22-rdf-syntax-ns#type
- http://www.w3.org/2002/07/owl#Class
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