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Kronisk granulomatös sjukdom, CGD - BLF

Kronisk granulomatös sjukdom, CGD - BLF

Kronisk granulomatös sjukdom, CGD - BLF

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Mutationer <strong>CGD</strong> Sverige<br />

X-bunden <strong>CGD</strong><br />

Samtliga mutationer unika förutom hos två bröder<br />

Punkt mutationer som leder till<br />

¨nonsense¨, ¨missense¨ och<br />

¨splice site¨ mutationer med ¨skipping¨ av exxon 2 o 6<br />

Insertion<br />

Total deletion med McCleod phenotyp, Kell negativ<br />

Unik 40 baspars duplikatur.<br />

Autosomal recessiv <strong>CGD</strong><br />

Av 7pat med p47 phox brist hade fyra en homozygot GT<br />

deletion<br />

2 hade heterozygot GT deletion

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