Report of two siblings with spondylodysplastic Ehlers-Danlos syndrome and B4GALT7 deficiency.
Delia LorenzWolfram KressAnn-Kathrin ZaumChristian P SpeerHelge HebestreitPublished in: BMC pediatrics (2021)
This is a first full report on two cases with spondylodysplastic Ehlers-Danlos syndrome and the c.723 + 4A > G variant of B4GALT7. The recurrent pneumothoraces observed in one case expand the variable phenotype of the syndrome.
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