Causes of Recurrent respiratory infections

Causes of the condition may include:¹ Causes of Recurrent Respiratory Infections:

• 19q13.11 Microdeletion Syndrome
• 2p15p16.1 Microdeletion Syndrome
• 3C Syndrome
• 48,XXXY Syndrome
• 48,XXYY Syndrome
• 49,XXXXY Syndrome
• Acroosteolysis Dominant Type
• Agammaglobulinemia 7, Autosomal Recessive
• Alopecia Antibody Deficiency
• Alpha-Mannosidosis
• Alstrom Syndrome
• Antisynthetase Syndrome
• Aortic Arch Defects
• Aspartylglucosaminuria
• Ataxia-Pancytopenia Syndrome
• Ataxia-Telangiectasia
• Attenuated Chediak-Higashi Syndrome
• Autosomal Agammaglobulinemia
• Autosomal Dominant Hyper-IgE Syndrome
• Autosomal Dominant Spondylocostal Dysostosis
• Autosomal Recessive Malignant Osteopetrosis
• Autosomal Recessive Robinow Syndrome
• Bardet-Biedl Syndrome 16
• Beta-Mannosidosis
• Bloom Syndrome
• Bone Dysplasia, Lethal Holmgren Type
• Brown-Vialetto-Van Laere Syndrome 1
• Card11 Immunodeficiency
• CD8 Deficiency, Familial
• Chediak-Higashi Syndrome
• Choreoacanthocytosis
• Choreoathetosis And Congenital Hypothyroidism With Or Without Pulmonarydysfunction
• Chromosome 18q Deletion Syndrome
• Chronic Granulomatous Disease
• Chronic Mucocutaneous Candidiasis
• Ciliary Dyskinesia, Primary, 12
• Ciliary Dyskinesia, Primary, 14
• Ciliary Dyskinesia, Primary, 15
• Ciliary Dyskinesia, Primary, 17
• Ciliary Dyskinesia, Primary, 2
• Ciliary Dyskinesia, Primary, 25
• Ciliary Dyskinesia, Primary, 29
• Ciliary Dyskinesia, Primary, 3
• Ciliary Dyskinesia, Primary, 32
• Ciliary Dyskinesia, Primary, 6
• Ciliary Dyskinesia, Primary, 7
• Cleidocranial Dysplasia
• Coffin-Siris Syndrome
• Combined Cellular And Humoral Immune Defects With Granulomas
• Congenital Disorder Of Glycosylation, Type IIj
• Congenital Disorder Of Glycosylation, Type Iv
• Congenital Fiber-Type Disproportion Myopathy
• Cortical Blindness-Intellectual Disability-Polydactyly Syndrome
• Cryptorchidism-Arachnodactyly-Intellectual Disability Syndrome
• Cutis Laxa
• Cutis Laxa, Autosomal Recessive, Type IA
• Cyclic Neutropenia
• Cystic Fibrosis
• Cystic Fibrosis-Gastritis-Megaloblastic Anemia Syndrome
• Cystic Hamartoma Of Lung And Kidney
• Dermatomyositis
• Diastrophic Dwarfism
• Distal 22q11.2 Microdeletion Syndrome
• Dyskeratosis Congenita
• Early Myoclonic Encephalopathy
• Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomaldominant
• Ectodermal Dysplasia-Blindness Syndrome
• Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome1
• Emanuel Syndrome
• Encephalopathy Due To Prosaposin Deficiency
• Epileptic Encephalopathy, Lennox-Gastaut Type
• Erythroderma, Congenital, With Palmoplantar Keratoderma, Hypotrichosis,And Hyper-Ige
• Erythromelalgia
• Facial Dysmorphism, Immunodeficiency, Livedo, And Short Stature
• Familial Dysautonomia
• Farber Disease
• Free Sialic Acid Storage Disease
• Fucosidosis
• Gamma-A-Globulin, Defect In Assembly Of
• Gamma-Heavy Chain Disease
• Gaucher Disease Type 2
• Gaucher Disease Type 3
• Glycogen Storage Disease Due To Acid Maltase Deficiency
• Glycogen Storage Disease Due To Glucose-6-Phosphatase Deficiency
• Glycogen Storage Disease II
• GM1 Gangliosidosis
• Good Syndrome
• Granulomatosis With Polyangiitis
• Hallermann-Streiff Syndrome
• Harlequin Ichthyosis
• Hereditary Folate Malabsorption
• Hereditary Mucoepithelial Dysplasia
• Hereditary Orotic Aciduria
• Hurler-Scheie Syndrome
• Hurler Syndrome
• Hypohidrotic Ectodermal Dysplasia-Hypothyroidism-Ciliary Dyskinesia Syndrome
• Hypomandibular Faciocranial Dysostosis
• Hypophosphatasia, Infantile
• ICF Syndrome
• Immunodeficiency 17
• Immunodeficiency 18
• Immunodeficiency 19
• Immunodeficiency 20
• Immunodeficiency 22
• Immunodeficiency 23
• Immunodeficiency 31C
• Immunodeficiency 35
• Immunodeficiency 36
• Immunodeficiency 41 With Lymphoproliferation And Autoimmunity
• Immunodeficiency 8
• Immunodeficiency, Common Variable, 10
• Immunodeficiency, Common Variable, 11
• Immunodeficiency, Common Variable, 5
• Immunodeficiency, Common Variable, 6
• Immunodeficiency, Common Variable, 7
• Immunodeficiency With Hyper-IgM, Type 2
• Immunoglobulin A Deficiency 1
• Intellectual Disability-Hypotonia-Skin Hyperpigmentation Syndrome
• Interstitial Lung Disease, Nephrotic Syndrome, And Epidermolysis Bullosa, Congenital
• Isolated Agammaglobulinemia
• Jacobsen Syndrome
• Jung-Wolff-Back-Stahl Syndrome
• Kleefstra Syndrome
• Krabbe Disease
• Lamellar Ichthyosis
• Larynx Atresia
• Leprechaunism
• Lichtenstein Syndrome
• Lipoid Proteinosis
• Locked-In Syndrome
• LUBS X-Linked Mental Retardation Syndrome
• Lymphangiectasia, Pulmonary, Congenital
• Lymphangioleiomyomatosis
• Macrosomia-Microphthalmia-Cleft Palate Syndrome
• Malt Lymphoma
• Martsolf Syndrome
• Meier-Gorlin Syndrome 6
• Melnick-Needles Syndrome
• Mental Retardation, Autosomal Dominant 40
• Mental Retardation, X-Linked 99, Syndromic, Female-Restricted
• Microcephalic Osteodysplastic Primordial Dwarfism Type II
• Microcephalic Primordial Dwarfism, Toriello Type
• Microcephaly, Epilepsy, And Diabetes Syndrome
• Minicore Myopathy With External Ophthalmoplegia
• Mucolipidosis Type II
• Mucopolysaccharidosis Type 1
• Mucopolysaccharidosis Type 7
• Mucus Inspissation Of Respiratory Tract
• Myoclonus, Hereditary, With Progressive Distal Muscular Atrophy
• Natural Killer Cell And Glucocorticoid Deficiency With DNA Repairdefect
• Netherton Syndrome
• Neutropenia, Severe Congenital, 4, Autosomal Recessive
• Neutropenia, Severe Congenital, 6, Autosomal Recessive
• Niemann-Pick Disease, Type A
• Niemann-Pick Disease, Type B
• Oculocerebrorenal Syndrome Of Lowe
• Opsismodysplasia
• Osteodysplasty, Precocious, Of Danks, Mayne, And Kozlowski
• Pantothenate Kinase-Associated Neurodegeneration
• Papillon-Lefevre Syndrome
• Paroxysmal Cold Hemoglobinuria
• Peho Syndrome
• Pelizaeus-Merzbacher Disease
• Prader-Willi Syndrome
• Primary Ciliary Dyskinesia
• Progeroid Syndrome, Neonatal
• Prolidase Deficiency
• Prune Belly Syndrome
• Pseudohypoaldosteronism, Type I, Autosomal Recessive
• Pulmonary Alveolar Proteinosis, Acquired
• Pulmonary Arterial Hypertension
• RAS-Associated Autoimmune Leukoproliferative Disorder
• Reticular Dysgenesis
• Retinitis Pigmentosa 6
• Sandhoff Disease
• Sanjad-Sakati Syndrome
• Seckel Syndrome 9
• Severe Combined Immunodeficiency
• Short-Limb Skeletal Dysplasia With Severe Combined Immunodeficiency
• Short-Rib Thoracic Dysplasia 11 With Or Without Polydactyly
• Short-Rib Thoracic Dysplasia 1 With Or Without Polydactyly
• Singleton-Merten Syndrome 1
• Spastic Paraplegia Type 2
• Spinal Muscular Atrophy, Type I
• Spinal Muscular Atrophy, Type II
• Spinocerebellar Ataxia, X-Linked 3
• Spondylocostal Dysostosis 2, Autosomal Recessive
• Spondylocostal Dysostosis, Autosomal Recessive 1
• Spondyloenchondrodysplasia With Immune Dysregulation
• Stevens-Johnson Syndrome
• Stickler Syndrome
• Sting-Associated Vasculopathy, Infantile-Onset
• Surfactant Metabolism Dysfunction, Pulmonary, 2
• Tay-Sachs Disease
• Tetrasomy 5p
• Thoracic Dysostosis, Isolated
• Total Anomalous Pulmonary Venous Return 1
• Trichorhinophalangeal Syndrome, Type I
• Vici Syndrome
• Williams Syndrome
• Wiskott-Aldrich Syndrome
• Wolf-Hirschhorn Syndrome
• X-Linked Intellectual Disability, Pai Type
• Xq28 (Mecp2) Duplication
• Yellow Nail Syndrome
• Zlotogora-Ogur Syndrome

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Back to: « Recurrent respiratory infections

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Causes List for Recurrent respiratory infections

Some of the possible causes of Recurrent respiratory infections or similar disorders may include:²

• AAT deficiency (Repeated lung infections)
• AIDS (recurrent colds)
• Absent corpus callosum cataract immunodeficiency (Recurrent respiratory infections)
• Achondroplasia and Swiss type agammaglobulinemia ...

... Full Causes List for Recurrent respiratory infections »

Causes

See also cause information for related diseases:

• Causes of Respiratory infection
• Causes of Common Cold
• Causes of Upper Respiratory Tract Infections
• Causes of Immune deficiency

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References

1. Source: Human Phenotype Ontology
2. Source: Algorithmically Generated List

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Note: This site is for informational purposes only and is not medical advice. See your doctor or other qualified medical professional for all your medical needs.