All individuals with variants in gene GUCY1A3

9 entries on 1 page. Showing entries 1 - 9.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00016849 - PubMed: Hervé 2014 2-generation family, 2 affected borthers, unaffected heterozygous carrier parents, brother of 24581742-Fam1Pat3 M yes France unknown - - - The individual was treated efficiently by nicardipine and perindopril for hypertension from the age of 20. MYMY6 0m: Achalasia; 3y: Stroke; Moyamoya or other intracranial angiopathy, Anterior circulation involvement, Posterior circulation involvement, Hypertension, Low platelet number, Platelet-aggregation abnormal 1 2 Marianne Vos (LOVD-team)
00016850 - PubMed: Hervé 2014 brother of 24581742-Fam1Pat1 M yes France unknown - - - - MYMY6 0m: Achalasia; (Mallignant)Hypertension, Raynaud phenomenon, Abnormal Platelet-aggregation, erectile dysfunction since adolescence 1 1 Marianne Vos (LOVD-team)
00016851 - PubMed: Hervé 2014 2-generation family, 2 affected sisters, unaffected heterozygous carrier parents, sister of 24581742-Fam2Pat2 F yes France unknown - - - - MYMY6 4m: Achalasia; Hypertension 1 2 Marianne Vos (LOVD-team)
00016852 - PubMed: Hervé 2014 sister of 24581742-Fam2Pat1 F yes France unknown - - - gastrostomy nutrition MYMY6 0d:regurgitation episodes; 7m: several episodes of right hemiparesis followed by generalized seizure, severe left hemiplegia, 2 large inffarcts, severe stenosis of both ICA bifurcations associated with moyamoya vessels on the left side; 11m: Achalasia; 3y: intense episode of microvascular dysfunction with cyanosis. These symptoms resolved spontaneously in a few hours; 4,5y:she remained severely disabled. She was able to pronounce only few words and to stay seated only for a few seconds.; 5y: stage 1 hypertension. Moyamoya or other intracranial angiopathy, Anterior circulation involvement, Posterior circulation involvement, Raynaud phenomenon, Livedo reticularis 1 1 Marianne Vos (LOVD-team)
00016853 - PubMed: Hervé 2014 2-generation family, 5 affected sibs (F, 4M), unaffected heterozygous carrier parents/sibs, brother of 24581742-Fam3PatIV9 M yes Algeria Algerian - - - Heller myotomy MYMY6 2y:right hemiparesis associated with aphasia; 6y:contralateral hemiparesis; 1y3m: Achalasia; Moyamoya or other intracranial angiopathy, Anterior circulation involvement 1 5 Marianne Vos (LOVD-team)
00016854 - PubMed: Hervé 2014 brother of 24581742-Fam3PatIV8 M yes Algeria Algerian - - - - MYMY6 2m: operated for achalasia; 4y7m:two episodes of transient right hemiparesis (left MCA infarct and an unusual intracranial angiopathy characterized by long arterial stenosis of the left MCA and ACA) 1 1 Marianne Vos (LOVD-team)
00016855 - PubMed: Hervé 2014 brother of 24581742-Fam3PatIV8 M yes Algeria Algerian - - - - MYMY6 Achalasia; No extra digestive investigation was realized in F3 IV-2, F3 IV-4, or F3 IV-5 in the absence of neurological symptoms. 1 1 Marianne Vos (LOVD-team)
00016856 - PubMed: Hervé 2014 brother of 24581742-Fam3PatIV8 M yes Algeria Algerian - - - - MYMY6 Achalasia; No extra digestive investigation was realized in F3 IV-2, F3 IV-4, or F3 IV-5 in the absence of neurological symptoms. 1 1 Marianne Vos (LOVD-team)
00016857 - PubMed: Hervé 2014 sister of 24581742-Fam3PatIV8 F yes Algeria Algerian ? - - Heller myotomy MYMY6 Achalasia; No extra digestive investigation was realized in F3 IV-2, F3 IV-4, or F3 IV-5 in the absence of neurological symptoms. 1 1 Marianne Vos (LOVD-team)
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.