Rare card

Sensenbrenner syndrome

Value

50 W

Attack

559

Defence

447

Players

0

Sensenbrenner syndrome (OMIM #218330) is a rare (less than 20 cases reported by 2010) ciliopathy first described by Judith A. Sensenbrenner in 1975. It is inherited in an autosomal recessive fashion, and is caused by a loss of function mutation in one of three genes: IFT122, IFT43, and WDR35.

Español