Vertaling van "members was actually " (Engels → Frans) :

TERMINOLOGIE

Syndrome with the association of diffuse palmoplantar keratoderma and acrocyanosis. It has been described in eight members of one family and in two sporadic cases. The mode of inheritance in the familial cases was autosomal dominant.
syndrome de kératodermie palmoplantaire diffuse-acrocyanose

X-linked mental retardation, Turner type has characteristics of moderate to severe intellectual deficit in boys and moderate intellectual deficit in girls. It has been described in 14 members from four generations of one family. Macrocephaly was repo
déficience intellectuelle liée à l'X type Turner