Traduction de «schwartz ocular syndrome » (Anglais → Français) :

Schwartz ocular syndrome

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syndrome oculaire de Schwartz

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

Schwartz-Bartter syndrome

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syndrome de Schwartz-Bartter

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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

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

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

Myotonia chondrodystrophica | osteochondromuscular dystrophy | Schwartz-Jampel- Aberfeld syndrome

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dystrophie ostéochondromusculaire | myopathie myotonique | myotonie chondrodystrophique | syndrome d’Aberfeld | syndrome Schwartz-Jampel

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Rare syndrome with the association of congenital nephrotic syndrome, ocular anomalies and microcoria. The disorder results in proteinuria with nephrotic syndrome and histological lesions marked by diffuse mesangial sclerosis. Ocular anomalies are pre

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syndrome de Pierson

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Aland Island eye disease [ Forsius-Eriksson syndrome | forsius-eriksson ocular albinism ]

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maladie des yeux d'Aland [ syndrome de Forsins-Eriksson ]

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ocular hypertelorism | hypertelorism | Greig's syndrome

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hypertélorisme oculaire | hypertélorisme | syndrome de Greig

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A very rare syndrome with characteristics of the association of Mobius syndrome (congenital facial palsy with impaired ocular abduction) with peripheral axonal neuropathy and hypogonadotropic hypogonadism. All of the reported cases were sporadic.

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syndrome de Moebius-neuropathie axonale-hypogonadisme hypogonadotrope

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infantile ocular muscle dystrophy | MOEBIUS Syndrom

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diplégie faciale congénitale | syndrome de Moebius

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'schwartz ocular syndrome' ->

Date index: 2022-02-06