The topic C1qD Disorder you are seeking is a synonym, or alternative name, or is closely related to the medical condition C1q Deficiency Disorder.

Quick Summary:

• C1q Deficiency Disorder is an infrequently occurring congenital disorder with manifestations that include recurrent skin lesions, long-term infections, and the presence of autoimmune disorders, chiefly systemic lupus erythematosus (SLE). It is informed that over 90% of the cases are associated with SLE
• C1q Deficiency Disorder is a genetic disorder with autosomal recessive pattern of inheritance. It is caused by mutations in the C1QA, C1QB, or C1QC genes. Due to this, the C1q protein complex important for complement system activation is either abnormal or deficient, causing a set of associated signs and symptoms
• C1q Deficiency Disorder leads to chronic infections, such as ear infection (otitis media), urinary tract infection (UTIs)s, and oral infections, apart from skin lesions in the form of small blisters that aggravate on exposure to light, cataract, loss of scalp hair, including chronic glomerulonephritis and kidney failure
• A management of C1q Deficiency Disorder depends on the presentations and complications. It may include stem cell transplantation. Systemic lupus erythematosus is treated using corticosteroids and immunosuppressive medications. With intensive medical therapy and for mild cases, the prognosis may be favorable

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