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Migration of an ancestral dysferlin splicing mutation from the Iberian peninsul...
Vernengo, Luis; Oliveira, Jorge; Krahn, Martin; Vieira, Emília; Santos, Rosário; Carraso, Luisa; Negrão, Luis; Panuncio, Ana; Leturcq, FranceMiyoshi myopathy, LGMD2B and DMAT are primary dysferlinopathies that belong to a group of muscular dystrophies inherited in an autosomal recessive mode. Additional presentations range from isolated hyperCKemia to severe functional disability. LGMD2B involves predominantly the proximal muscles of the lower limbs whereas in Miyoshi myopathy the muscles involved are those of the posterior muscle compartment of the...
Tetra-amelia and lung hypo/aplasia syndrome: New case report and review
Sousa, Sérgio B.; Pina, Raquel; Ramos, Lina; Pereira, Naigel; Krahn, Martin; Borozdin, Wiktor; Kohlhase, Jürgen; Amorim, Marta; Gonnet, KatiaTetra-amelia is a rare malformation that may be associated with other anomalies and is usually inherited in an autosomal recessive pattern. We describe a fetus, born to a nonconsanguineous couple, with tetra-amelia, bilateral cleft lip and palate and bilateral lung agenesis, without other anomalies. Karyotype was normal (46,XX) and premature centromere separation was excluded. No mutation was identified upon mo...
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