Background: Cerebrotendinous xanthomatosis is a rare autosomal recessive neurometabolic disorder characterized by chronic diarrhea, tendon xanthomas, juvenile cataracts, and neurological symptoms. Case Report: An adult patient with cerebrotendinous xanthomatosis exhibited ataxia and palatal tremor in the absence of tendon xanthomas and cataracts. Discussion: The importance of this case resides on the fact that cerebrotendinous xanthomatosis should be considered as a possible etiology of the syndrome of progressive ataxia with palatal tremor, even in the absence of tendon xanthomas and cataracts. Early diagnosis is critical to the institution of specific treatment with chenodeoxycholic acid
Classic cerebrotendinous xanthomatosis (CTX; OMIM #213700) manifests with chronic diarrhea, juvenile...
Introduction: Xeroderma pigmentosum (XP) is a rare autosomal recessive disorder of DNA repair, with ...
The final publication is available at Springer via doi: 10.1007/s00415-013-7136-
Background: Cerebrotendinous xanthomatosis is a rare autosomal recessive neurometabolic disorder cha...
Cerebrotendinous xanthomatosis (CTX) is a rare hereditary neuro-metabolic disease in which depositio...
Background: The pathophysiology of the movement disorder progressive ataxia with palatal tremor (PAP...
Background: Abetalipoproteinemia is a rare disorder of fat absorption, characterized by vitamin defi...
Introduction: Identifying the underlying etiology of nonfamilial adult-onset progressive cerebellar ...
Background: Progressive ataxia and palatal tremor (PAPT) can be observed in both acquired brainstem ...
Background: Spontaneous intracranial hypotension (SIH) is a clinically variable syndrome caused by l...
Cerebrotendinous Xanthomatosis(CTX) is an uncommon autosomal recessive disorder in which there is ac...
Background: The pathophysiology of the movement disorder progressive ataxia with palatal tremor (PAP...
Cerebrotendinous xanthomatosis is an autosomal recessive disorder of bile acid metabolism causing a ...
Cerebrotendinous xanthomatosis (CTX) is a treatable disorder of bile acid production caused by mutat...
Background: Both hypothyroidism and Hashimoto's thyroiditis (HT) can rarely be associated with cereb...
Classic cerebrotendinous xanthomatosis (CTX; OMIM #213700) manifests with chronic diarrhea, juvenile...
Introduction: Xeroderma pigmentosum (XP) is a rare autosomal recessive disorder of DNA repair, with ...
The final publication is available at Springer via doi: 10.1007/s00415-013-7136-
Background: Cerebrotendinous xanthomatosis is a rare autosomal recessive neurometabolic disorder cha...
Cerebrotendinous xanthomatosis (CTX) is a rare hereditary neuro-metabolic disease in which depositio...
Background: The pathophysiology of the movement disorder progressive ataxia with palatal tremor (PAP...
Background: Abetalipoproteinemia is a rare disorder of fat absorption, characterized by vitamin defi...
Introduction: Identifying the underlying etiology of nonfamilial adult-onset progressive cerebellar ...
Background: Progressive ataxia and palatal tremor (PAPT) can be observed in both acquired brainstem ...
Background: Spontaneous intracranial hypotension (SIH) is a clinically variable syndrome caused by l...
Cerebrotendinous Xanthomatosis(CTX) is an uncommon autosomal recessive disorder in which there is ac...
Background: The pathophysiology of the movement disorder progressive ataxia with palatal tremor (PAP...
Cerebrotendinous xanthomatosis is an autosomal recessive disorder of bile acid metabolism causing a ...
Cerebrotendinous xanthomatosis (CTX) is a treatable disorder of bile acid production caused by mutat...
Background: Both hypothyroidism and Hashimoto's thyroiditis (HT) can rarely be associated with cereb...
Classic cerebrotendinous xanthomatosis (CTX; OMIM #213700) manifests with chronic diarrhea, juvenile...
Introduction: Xeroderma pigmentosum (XP) is a rare autosomal recessive disorder of DNA repair, with ...
The final publication is available at Springer via doi: 10.1007/s00415-013-7136-