Create issue ticket

13 Possible Causes for Dysmetria, Microcephaly (2-3 SD)

Did you mean: Dysmetria, Microcephaly (2-3 SD

  • Dysequilibrium Syndrome

    Microcephaly (-3 to -4 SD below the mean) has been reported in a few affected individuals. Life span.[ncbi.nlm.nih.gov] Short stature (height just below the 2 nd centile) is a feature in a few affected individuals. Deep tendon reflexes in the lower extremities tend to be brisk.[ncbi.nlm.nih.gov]

  • Severe Neonatal-Onset Encephalopathy with Microcephaly

    […] eye movement Aggressive behavior Hyperhidrosis Talipes equinovarus Muscular hypotonia Visual impairment Dysphagia Congenital muscular dystrophy Poor speech Polyneuropathy Dysmetria[mendelian.co] Discussion Microcephaly is usually defined as an occipitofrontal head circumference (OFC) more than 2 standard deviations (SD) below the mean for sex, age and ethnicity.[pediatriceducation.org] The adult and childhood phenotype is characterized by visual loss due to retinitis pigmentosa, progressive ataxia, dysmetria, intention tremor, dysarthria, dysphagia, and[cerebellumandataxias.biomedcentral.com]

  • Autosomal Dominant Mental Retardation 28

    […] subtype of autosomal dominant cerebellar ataxia type 1, characterized by the adult-onset of unsteady gait and dysarthria, followed by wide-based gait, gait ataxia, ocular dysmetria[mendelian.co] A common finding in microcephaly is also short stature, typically between -1 SD and -2 SD and in Seckel syndrome it ranges between -4 and -12 SD 3.[centogene.com] Extensor Course: Progressive & Disabling in 2nd & 3rd decade in some patients Cerebellar Spastic-Ataxic gait EOM: Gaze-evoked horizontal nystagmus; Upbeat nystagmus; Ocular dysmetria[neuromuscular.wustl.edu]

  • Autosomal Dominant Mental Retardation 21

    […] is a rare, genetic neurological disease, due to SPTBN2 mutations, characterized by global development delay in infancy, followed by childhood-onset gait ataxia with limb dysmetria[mendelian.co] A common finding in microcephaly is also short stature, typically between -1 SD and -2 SD and in Seckel syndrome it ranges between -4 and -12 SD 3.[centogene.com] Hypometric saccades Abnormal cerebellum morphology Impaired vibratory sensation Diffuse cerebellar atrophy Morphological abnormality of the pyramidal tract Titubation Limb dysmetria[mendelian.co]

  • Bilateral Temporo-Occipital Polymicrogyria

    All three had esotropia, increased muscle tone, mild truncal ataxia, and finger dysmetria, without dysmorphic features or other congenital anomalies.[cags.org.ae] ., head circumference 3 SD and MIC severe microcephaly (i.e., birth head circumference MAC macrocephaly (i.e., head circumference 97%) 3.[ncbi.nlm.nih.gov] […] parietal, parieto oc- age 9 mo; EEG that shows cipital multifocal spikes, diffuse Severe global delay; hypotonia of legs more than slow waves. arms; hyperreflexia, nystagmus, dysmetria[fliphtml5.com]

  • Autosomal Dominant Congenital Nystagmus 3

    Results: Examination of the family showed that all affected members had gait ataxia and cognitive disability with variable features of dysarthria, dysmetria, dysdiadochokinesia[neurology.org] Sheriff and Hegab (1988) described a Kuwaiti family in which 3 sibs, 2 boys and a girl, had true microcepha...[findzebra.com] Saccadic dysmetria from vermis lesions can assume a number of patterns (37).[neuroophthalmology.ca]

  • Autosomal Recessive Mental Retardation Type 3

    They may also have difficulty with movements that involve judging distance or scale ( dysmetria ).[en.wikipedia.org] […] reviews BIALLELIC, autosomal or pseudoautosomal Sources Expert Review Green NHS GMS Other Phenotypes Microcephaly, epilepsy, and diabetes syndrome, 614231 Microcephaly (-3[panelapp.genomicsengland.co.uk] […] is a rare, genetic neurological disease, due to SPTBN2 mutations, characterized by global development delay in infancy, followed by childhood-onset gait ataxia with limb dysmetria[mendelian.co]

  • Cataract - Ataxia - Short Stature - Mental Retardation (CASM)

    Extensor Course: Progressive & Disabling in 2nd & 3rd decade in some patients Cerebellar Spastic-Ataxic gait EOM: Gaze-evoked horizontal nystagmus; Upbeat nystagmus; Ocular dysmetria[neuromuscular.wustl.edu] […] reviews BIALLELIC, autosomal or pseudoautosomal Sources Expert Review Green NHS GMS Other Phenotypes Microcephaly, epilepsy, and diabetes syndrome, 614231 Microcephaly (-3[panelapp.genomicsengland.co.uk] At age 6 years, she had severe spasticity of the legs, mild intention tremor, dysmetria, dysarthria, and nystagmus.[findzebra.com]

  • Autosomal Recessive Mental Retardation Type 27

    Tremor, dysmetria, and poor coordination of fine movements are often present. A sensorineural hearing loss has been found in several individuals.[disorders.eyes.arizona.edu] A common finding in microcephaly is also short stature, typically between -1 SD and -2 SD and in Seckel syndrome it ranges between -4 and -12 SD 3.[centogene.com] Through examination, the modality of limb motion should be observed, and any impairment of voluntary movement, including dysmetria, athetosis, or dystonia, must be assessed[genecelltissue.com]

  • Brain Calcification Type Rajab

    Hypoglycorrhachia Jerky head movements Focal seizures without impairment of consciousness or awareness Paroxysmal dystonia Paroxysmal dyskinesia Nausea Limb dysmetria Abnormality[mendelian.co] Summary of Clinical Features of Affected PatientsPatient1 2 3 4 5 6 7 8Widespread braincalcifications Microcephaly(2 to 3 SD) Postnatal growth delay Short stature Thin build[docslide.com.br] Summary of Clinical Features of Affected Patients Patient 1 2 3 4 5 6 7 8Widespread brain calcifications Microcephaly(2 to 3 SD) Postnatal growth delay Short stature Thin[docslide.net]

Further symptoms

Similar symptoms