Phenotypes for disease #00422 (DPDD (dihydropyrimidine dehydrogenase deficiency (DPDD)), OMIM:274270)

12 entries on 1 page. Showing entries 1 - 12.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Enzyme/Activity     

Protein     

Owner     

Individual ID     
0000015947 - - - Familial - - - - undetectable (leukocytes) - Johan den Dunnen 00017586
0000015948 partial deficiency - - Familial - - - - <0.10 (PBM cells) - Johan den Dunnen 00017588
0000015949 partial deficiency - - Familial - - - - 0.3 (PBM cells) - Johan den Dunnen 00017589
0000015950 carcinoma, basal cell; severe toxicity from 5-FU treatment - - Isolated (sporadic) 76y - - - undetectable (PBM cells) - Johan den Dunnen 00017591
0000015951 partial deficiency, index case 5-FU toxicity from cancer treatment - - Familial, autosomal dominant - - - - 0.65 (PBM cells) - Johan den Dunnen 00017592
0000015952 8y-severe growth retardation (length <3rd centile), submitted to hospital for treatment of upper airway infection, hypokalaemia (2.5mmol/L), thymine-uraciluria, no convulsions or other neurological abnormalities - - Isolated (sporadic) - - - - undetectable (fibroblasts) - Johan den Dunnen 00017593
0000015953 9m-febrile convulsions, severe neuromotor retardation, spastic tetraplegia, cerebral MRI ventriculomegaly with white-matter hypodensity microcephaly, growth retardation; 6y- thymine-uraciluria - - Isolated (sporadic) - - - - <0.01 (fibroblasts) - Johan den Dunnen 00017594
0000015954 - - - Isolated (sporadic) - - - - undetectable (fibroblasts) - Johan den Dunnen 00017595
0000128119 see paper; ..., healthy, history of gastrointestinal dysmotility, normal development, normal intellect, significant pregnancy-induced symptoms (severe abdominal pain, increased gastrointestinal symptoms, pancreatitis, intermittent changes in consciousness) in three consecutive pregnancies; 3rd pregnancy developed recurrent stroke-like episodes including symptoms of headaches, blurring to near loss of vision, and right hemiparesis dihydropyrimidine dehydrogenase deficiency DPDD Familial, autosomal recessive - - - - - - Maja Tarailo-Graovac 00155716
0000172603 see paper; ..., born with apparent cortical blindness, subsequently exhibited severe developmental delay; 2y-severe spasticity, hyperreflexia felt secondary to intrauterine stroke; multiple brain MRIs delay in myelination; 18y-spastic paraparesis, mild intellectual disability - DPDD Familial, autosomal recessive 18y - - - - - Johan den Dunnen 00228665
0000172604 see paper; ..., congenital blindness delayed early gross motor and social milestones; 8m-visual impairment improved, development normalized; 10's-gastrointestinal dysmotility; 19y-intellectually normal - DPDD Familial, autosomal recessive 19y - - - - - Johan den Dunnen 00228666
0000223046 - Rectal cancer DPD deficiency Unknown - - - >54 Decreased - Nedal Bukhari 00289434
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