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Fig. 1 | Allergy, Asthma & Clinical Immunology

Fig. 1

From: A novel mutation in NCF2 resulting in very-early-onset colitis and juvenile idiopathic arthritis in a patient with chronic granulomatous disease

Fig. 1

Deficiency of p67phox in a child with AR CGD. a Family pedigree. The arrow indicates the proband. Each generation is designated by a Roman numeral (I, II). Blackened symbols denote the affected family members. m mutation, WT wild type. b Scars of previous surgically drained perianal abscesses and a perianal fistula opening at the 12 o’clock position (arrow)

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Allergy, Asthma & Clinical Immunology

ISSN: 1710-1492

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