When a child is first diagnosed with chronic granulomatous disease (CGD), it can shock families and bring up challenging emotions. Many parents experience anxiety and depression, as they’ve watched their child struggle for months or years with infections, surgeries, and hospitalizations, only to be told that the cause is CGD. CGD is a
Read MoreUpdate Prior research studies have shown that female X-linked carriers of chronic granulomatous disease (CGD) – mothers, daughters, sisters, aunts, and grandmothers – exhibit some symptoms related to the disease. The most common are discoid lupus (which causes round lesions on the skin), mouth ulcers, and joint pain. But a new study that
Read MoreMutations in genes of persons with chronic granulomatous disease (CGD) affect the person’s production of superoxide, which in turn dictates the severity of CGD symptoms, according to a review of CGD by Dr. Jennifer Leiding and Dr. Steven Holland for the National Institute of Health’s National Library of Medicine. The six genes that can be
Read MoreFor over a year, Diane Mato repeatedly took her toddler son Nicholas to doctors because of fevers that lasted weeks and severe urological problems that required a painful scope in his bladder and a catheter. The Mato family includes, from left, dad Manny, Nicholas, Adrian, mom Diane, and Eric. When symptoms returned despite the medical
Read MoreA PBS health program focusing on chronic granulomatous disease (CGD) is now available on YouTube. Part of the PBS Exploration Health educational series, the 15-minute piece examines the science of chronic granulomatous disease (CGD), profiles persons living with CGD, interviews doctors serving the CGD community, and explores the various
Read MoreLiving with CGD is a program of the Immune Deficiency Foundation. This site is made possible by an unrestricted educational grant from:
