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DCM3 carrier
Acral mutilation syndrome (AMS) is a neurological disease characterized by insensitivity to pain in peripheral parts of the body (limbs
uterine body
Schwierigkeiten beim Stehen und Gehen in einer geraden Linie
Polyneuropathie 1 (LPN1) - Leonberger Searchterm DCM3 carrierLeonberger Polyneuropathy 1 (LPN1) is a polyneuropathy condition (PN) that is associated with a mutation in ARHGEF10 gene. A loss of function of the gene may lead to the loss of proper nerve signalling. Polyneuropathy can display a wide range of age of onset and may appear due to the mutations in other genes (GJA9, NDRG1) with a different mode of inheritance. Clinical signs include generalized weakness, hypotonia, muscle atrophy secondary to
