A rare neurologic disease characterized by global developmental delay, intellectual disability, multiple ischemic lesions on brain MRI, behavioral abnormalities, dystonia, choreic movements and pyramidal syndrome, facial dysmorphism (hypertelorism, a

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

syndrome autosomique récessif de leucoencéphalopathie-infarctus cérébraux-rétinite pigmentaire

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

A rare chromosomal anomaly syndrome with principle characteristics of intrauterine growth restriction, congenital cardiac anomalies (ventricular and atrial septal defects, patent ductus arteriosus) and craniofacial dysmorphism (hypertelorism, downsla

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

trisomie 15 en mosaïque

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

A rare multiple congenital anomalies syndrome with characteristics of mild intellectual disability, short stature, cardiac anomalies, mild dysmorphic features (macrocephaly, prominent forehead, hypertelorism, exophthalmos), cutis laxa, joint hyperlax

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

syndrome cranio-facio-fronto-digital

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

Greig hypertelorism

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

hypertélorisme de Greig

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]

hypertelorism

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

hypertélorisme

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]

hereditary nephropathy | Alport's syndrome | hereditary haematuria associated with nerve deafness and ocular changes | hereditary hematuria associated with nerve deafness and ocular changes | hereditary nephropathy with haematuria | familial hereditary nephropathy | haematuric familial nephropathy

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

néphropathie familiale avec surdité | syndrome d'Alport | néphrite hématurique héréditaire avec surdité | néphrite chronique héréditaire

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]

D'autres ont cherché : alport's syndrome greig hypertelorism greig's syndrome afocal ocular familial hereditary nephropathy haematuric familial nephropathy hereditary nephropathy hereditary nephropathy with haematuria hypertelorism non-corrective ocular ocular hypertelorism ocular motoricity ocular motricity orbital hypertelorism plano ocular total ocular motility Ocular hypertelorism

datacenter (1): www.wordscope.fr (v4.0.br)

'Ocular hypertelorism' ->

Date index: 2021-04-19