- latent nystagmus
- nystagmus that occurs only when one eye is covered.
Medical dictionary. 2011.
Medical dictionary. 2011.
Nystagmus — Horizontal optokinetic nystagmus, a normal (physiological) form of nystagmus ICD 10 H55, H81.4 … Wikipedia
Nystagmus — Rapid rhythmic repetitious involuntary (unwilled) eye movements. Nystagmus can be horizontal, vertical or rotary. * * * Involuntary rhythmic oscillation of the eyeballs, either pendular or with a slow and fast component. [G. nystagmos, a nodding … Medical dictionary
Pathologic nystagmus — ICDO = OMIM = MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = D009759 Pathologic nystagmus is a form of involuntary eye movement. It is characterized by alternating smooth pursuit in one direction and saccadic movement in the other… … Wikipedia
Infantile esotropia — is an ocular condition of early onset in which one or either eye turns inward. It is a specific sub type of esotropia and has been a subject of much debate amongst ophthalmologists with regard to its naming, diagnostic features, and treatment.… … Wikipedia
Esotropia — Classification and external resources ICD 10 H50.0, H50.3 ICD 9 … Wikipedia
Dissociated Vertical Deviation — Dissociated Vertical Deviation(DVD) is an ocular condition which occurs in association with a squint, typically Infantile Esotropia. Patients with DVD show an upward movement of one eye when the eye is covered (i.e. when the two eyes are… … Wikipedia
Dissociated vertical deviation — (DVD) is an ocular condition which occurs in association with a squint, typically Infantile Esotropia. Contents 1 Mechanism 2 Characteristics 3 Differential Diagnosis … Wikipedia
MLN — manifest latent nystagmus; membranous lupus nephropathy; mesenteric lymph node; motilin … Medical dictionary
nistagmo latente — Eng. Latent nystagmus Nistagmo que aparece únicamente cuando se ocluye el ojo … Diccionario de oftalmología
Forsius-Eriksson syndrome — X linked tapetoretinal degeneration, formerly thought to be a form of ocular albinism, caused by a mutation in the CACNA1F gene (locus: Xp11.23), which encodes a voltage gated calcium channel subunit. Symptomatic males exhibit foveal hypoplasia,… … Medical dictionary