Harrington syndrome also called as
DiGeorge syndrome is a congenital
immunodeficiency characterized by abnormal facies, congenital heart defects,
hypoparathyroidism with hypocalcaemia, cognitive, behavioral, and psychiatric problems, and increased susceptibility to infections.
Causes
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Harrington syndrome is found to have a microdeletion of 22q11.
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Particularly affecting development of the third and fourth branchial pouches (pharyngeal pouches).
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This affects the thymus gland and parathyroid glands, responsible for regulation of blood calcium levels.
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It’s inherited as autosomal dominant, autosomal recessive and X-linked fashions.
Signs and symptoms
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Endocrine- Hypoparathyroidism leading to hypocalcaemia usually begins in the neonatal period, occasionally manifesting in the form of tetany or tonic convulsions.
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Palatal abnormalities- cleft palate, submucosal cleft palate, and velopharyngeal incompetence
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Immunology- Thymic hypoplasia or aplasia leading to defective T-cell function is the hallmark of DiGeorge anomaly.
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Hearing loss- conductive and sensorineural hearing loss
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Other manifestations- growth retardation, behavioral, psychiatric, , communication disorders, and significant feeding problems
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Infections- Increased susceptibility to infections like pneumocystis carinii, fungal infections and viral infections
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Association with other autoimmune disease- Graves disease, rheumatoid arthritis, and immune thrombocytopenic purpura
Tests and diagnosis
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Micro deletion of chromosomes can usually be detected in 2-3 days by fluorescent in situ hybridization (FISH) and rapid PCR techniques
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Assessment of parathyroid function – Low calcium levels
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Lateral view of chest X-ray- Thymic aplasia or hypoplasia
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2D- echo to detect cardiac anomolies
Treatment
Hypoparathyroidism and hypocalcemia are managed with calcium and vitamin D administration.
Treatment of immunodeficiency- Early thymus transplantation (ie, before the onset of infectious complications) may promote successful immune reconstitution.
Surgical care- Correct cardiac malformations per standard surgical techniques. Obtain early consultation with a cardiologist and immunologist to evaluate disease manifestations.