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swallowing difficulty
May-Hegglin Anomaly (MHA) is a hereditary disorder described in Pugs
Once affected puppies are transferred to a solid diet with digestive enzyme supplementation
Foetal onset neuroaxonal dystrophy (FNAD) is a fatal autosomal recessive dystrophy of the central and/or peripheral nervous system
Narcolepsy is an autosomal recessive disorder of sleeping
Hypophosphatasie (HPP) Startseite swallowing difficultyHypophosphatasia (HPP) is a rare canine autosomal recessive disease affecting bone and cartilage tissues. The symptoms include skeletal hypomineralisation, growth retardation, short stature, hypotonia, fractures, seizures and movement difficulties, meanwhile the cognition remains unharmed. Affected individuals can be stillborn or they develop mild to aggressive symptoms in the adulthood. Inheritance: autosomal recessive Mutation: ALPL gene Genetic
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