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3,319 Possible Causes for Abnormal Gait, Microcephaly (2-3 SD), Ocular Muscle Palsies

Did you mean: Abnormal Gait, Microcephaly (2-3 SD, Ocular Muscle Palsies

  • Dysequilibrium Syndrome

    ICD-10-CM Diagnosis Code R26.89 Other abnormalities of gait and mobility 2016 2017 2018 2019 Billable/Specific Code electrolyte E87.8 Syndrome - see also Disease disequilibrium[] Microcephaly (-3 to -4 SD below the mean) has been reported in a few affected individuals. Life span.[] , inconclusive, without diagnosis - see also Abnormal bicarbonate E87.8 chloride E87.8 Hyperchloremia E87.8 Hyperelectrolytemia E87.8 Hypochloremia E87.8 Imbalance R26.89[]

  • Hydrocephalus

    ., congenital toxoplasmosis (see congenital infections ) Acquired Clinical features Features of increased ICP Headache, nausea, and vomiting Papilledema Abnormal gait Impaired[] Other symptoms include abnormal gait (difficulty walking), inability to hold urine ( urinary incontinence ), and, occasionally, inability to control the bowels.[]

    Missing: Microcephaly (2-3 SD)
  • Wernicke Encephalopathy

    Wernicke encephalopathy (WE) commonly presents with oculomotor abnormalities, gait ataxia and confusion.[] . - Ocular: pupillary changes. Extraocular muscle palsy; gaze palsy: nystagmus. Hypothalamus.[] The diagnosis was supported by abnormal serum thiamine and disappearance of the gait disturbance after administration of intravenous thiamine.[]

    Missing: Microcephaly (2-3 SD)
  • Multiple Sclerosis

    abnormalities (e.g. wide-based gait, limb ataxia, slapping foot) joint or muscle contractures neurological examination muscle spasticity increased deep tendon reflexes muscle[] Vertigo, incoordination and other cerebellar problems, depression, emotional lability, abnormalities in gait, dysarthria, fatigue and pain are also commonly seen.[] Difficulty walking Difficulty walking can occur with MS for a number of reasons: numbness in your legs or feet difficulty balancing muscle weakness muscle spasticity difficulty[]

    Missing: Microcephaly (2-3 SD)
  • Subacute Combined Degeneration of Spinal Cord

    Numbness of the limbs and trunk is an early symptom; weakness, clumsiness and spasticity, abnormal reflexes, gait ataxia develop later.[] Gait was unremarkable, reflexes were normal: There were no pyramidal tract symptoms, no pareses and no mental abnormalities.[] […] of the gait.[]

    Missing: Microcephaly (2-3 SD)
  • Machado-Joseph Disease

    walking due to muscle spasms (spastic gait) Poor reflexes Type III (MJD-III) Between 40-70 years of age Symptoms slowly worsen over time Muscle twitching Numbness, tingling[] The majority of patients develop gait abnormalities and a series of other neurological symptoms between the ages of 20 and 40.[] We describe three patients with the Machado-Joseph disease (MJD) genetic abnormality who had non-movement disorder neurological symptoms or signs that preceded the gait ataxia[]

    Missing: Microcephaly (2-3 SD)
  • Myasthenia Gravis

    Other symptoms include: Changes in facial expression Difficulty chewing Difficulty speaking Difficulty swallowing Difficulty walking or doing repetitive work with arms and[] Its main symptoms, which the ophthalmologist may encounter, are ptosis, diplopia, variable extra-ocular muscle palsies or incomitant strabismus, and external ophthalmoplegia[] , and beginning cranial nerve palsy showing dysarthrophonia, facial paralysis, and eye movement abnormalities and was diagnosed as rapid onset (atypical) CIDP.[]

    Missing: Microcephaly (2-3 SD)
  • Abetalipoproteinemia

    walking by the time they turn 10 years.[] […] problems with sensing temperature and touch –– especially in the hands and feet (hypesthesia) Trouble walking ( ataxia ): Approximately 33 percent of children will have difficulty[] Affected individuals experience progressive neurological deterioration, muscle weakness, difficulty walking, and blood abnormalities including a condition in which the red[]

    Missing: Microcephaly (2-3 SD)
  • Blepharofacioskeletal Syndrome

    Brachydactyly Malar flattening Bulbous nose Arachnodactyly Death in infancy Cupped ear Motor delay Short nose Inability to walk Congenital onset Joint laxity Deeply set eye Abnormal[] […] at 2y)SmitheLemlieOpitzsyndrome[Porter, 2008]Short Stature (8 SD) (7 SD) Microcephaly (3 SD) (3 SD) Failure to gain weight Low birth weight Skin abnormalities Transient non-pitting[] Dysarthria, sialorrhea and personality change, gait abnormalities and arm tremor account for the majority of presenting symptoms and signs.[]

  • Miller-Fisher Syndrome

    We describe an 11-year-old female patient who presented with a 7-day history of diplopia and difficulty walking.[] He had no limb ataxia but exhibited a slightly wide-based gait with difficulty walking heel-to-toe.[] Patients typically seek medical attention because of rapid decrease in vision over days and/or difficulty walking.[]

    Missing: Microcephaly (2-3 SD)

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