Abstract Adenosine kinase (ADK) deficiency is a very rare inborn error of methionine and adenosine metabolism. It is characterized by developmental delay, hypotonia, epilepsy, facial dysmorphism, failure to thrive, transient liver dysfunction with cholestasis, recurrent hypoglycemia, and cardiac defects. Only 26 cases (16 families) of ADK deficiency have been published since its identification in 2011. Vascular abnormalities in cervical arteries and cerebral stroke have never been reported in this condition. Here, we describe two patients with ADK deficiency and vascular tortuosity leading to stroke in one of them. ADK deficiency is a rare inborn error of methionine metabolism with a complex phenotype that might be associated with cerebrova...
A deficiency of adenylosuccinate lyase (ASDL) is characterised by the accumulation of SAICAriboside ...
The deficiency of adenosine deaminase 2 (DADA2) is an autosomal recessively inherited disease that h...
ObjectiveDescribe the clinical characteristics and histopathology findings in a family with two sibl...
Adenosine kinase (ADK) deficiency (OMIM [online mendelian inheritance in man]: 614300) is an autosom...
BACKGROUND: Adenosine kinase deficiency is a recently described defect affecting methionine metaboli...
Adenosine kinase deficiency (ADK deficiency) is a recently described disorder of methionine and aden...
SUMMARY: Adenosine deaminase 2 deficiency (OMIM #615688) is an autosomal recessive disorder characte...
Abstract Adenosine kinase (ADK) deficiency is a rare autosomal recessive inborn error of metabolism ...
BACKGROUND: Patients with adenosine deaminase 2 (ADA2) deficiency can present with various neurologi...
Adenosine kinase (ADK) deficiency is a rare inborn error of methionine and adenosine metabolism. So ...
Deficiency of adenosine deaminase 2 (DADA2) is a unique monogenic autoinflammatory disease caused by...
BACKGROUND: Patients with adenosine deaminase 2 (ADA2) deficiency can present with various neurologi...
Adenosine is an endogenous neuromodulator with anticonvulsive and neuroprotective activity. Adenosin...
Abstract Background Adenosine deaminase 2 (ADA2) deficiency is an inherited autoinflammatory syndrom...
Most cases of adenylosuccinate lyase (ADSL OMIM 103050) deficiency reported to date are confined to ...
A deficiency of adenylosuccinate lyase (ASDL) is characterised by the accumulation of SAICAriboside ...
The deficiency of adenosine deaminase 2 (DADA2) is an autosomal recessively inherited disease that h...
ObjectiveDescribe the clinical characteristics and histopathology findings in a family with two sibl...
Adenosine kinase (ADK) deficiency (OMIM [online mendelian inheritance in man]: 614300) is an autosom...
BACKGROUND: Adenosine kinase deficiency is a recently described defect affecting methionine metaboli...
Adenosine kinase deficiency (ADK deficiency) is a recently described disorder of methionine and aden...
SUMMARY: Adenosine deaminase 2 deficiency (OMIM #615688) is an autosomal recessive disorder characte...
Abstract Adenosine kinase (ADK) deficiency is a rare autosomal recessive inborn error of metabolism ...
BACKGROUND: Patients with adenosine deaminase 2 (ADA2) deficiency can present with various neurologi...
Adenosine kinase (ADK) deficiency is a rare inborn error of methionine and adenosine metabolism. So ...
Deficiency of adenosine deaminase 2 (DADA2) is a unique monogenic autoinflammatory disease caused by...
BACKGROUND: Patients with adenosine deaminase 2 (ADA2) deficiency can present with various neurologi...
Adenosine is an endogenous neuromodulator with anticonvulsive and neuroprotective activity. Adenosin...
Abstract Background Adenosine deaminase 2 (ADA2) deficiency is an inherited autoinflammatory syndrom...
Most cases of adenylosuccinate lyase (ADSL OMIM 103050) deficiency reported to date are confined to ...
A deficiency of adenylosuccinate lyase (ASDL) is characterised by the accumulation of SAICAriboside ...
The deficiency of adenosine deaminase 2 (DADA2) is an autosomal recessively inherited disease that h...
ObjectiveDescribe the clinical characteristics and histopathology findings in a family with two sibl...