Create issue ticket

1,221 Possible Causes for Cerebellar Signs during Episodes, Cognitive Developmental Delay

  • Iron Deficiency

    The latter include decreased aerobic work performance, hair loss, developmental delay, cognitive and intellectual impairment, adverse pregnancy outcome, and impaired immune[] Reversal of developmental delays in iron-deficient anaemic infants treated with iron. Lancet 1993;341(8836):1-4. Lozoff B, Jimenez E, Wolf AW.[] Iron deficiency and cognitive function. Annu Rev Nutr 1993;13:521-37. Idjradinata P, Pollitt E.[]

    Missing: Cerebellar Signs during Episodes
  • Hartnup Disease

    However, some people with Hartnup disease have episodes during which they exhibit other signs, which can include skin rashes; difficulty coordinating movements ( cerebellar[] For most affected individuals, this is the only sign of the condition.[] These episodes are typically temporary and are often triggered by illness, stress, nutrient-poor diet, or fever.[]

  • Waisman Syndrome

    delay, cognitive impairment, macroencephaly, and, in some, seizures; EO parkinsonism with tremor appeared subsequently as the presenting symptom.[] […] phenotype in individuals with Down syndrome that includes significant delay in nonverbal cognitive development accompanied by additional, specific deficits in speech, language[] The symptoms are similar: developmental delays gr oss and fine motor skill delays speech and language delays learning and behavior problems hyperextensible joints anxiety[]

    Missing: Cerebellar Signs during Episodes
  • Early Infantile Epileptic Encephalopathy Type 2

    Patients with a SYNGAP1 mutation have a developmental delay, cognitive regression and some patients have a autism.[] developmental delay and intellectual disability.[] […] and motor development and often result in a devastating permanent global developmental delay and intellectual disability.[]

    Missing: Cerebellar Signs during Episodes
  • Early Infantile Epileptic Encephalopathy Type 17

    […] featuring moderate developmental delay associated with complex stereotypies, mainly facial dyskinesia, and mild epilepsy.[] Clinical features range from severe motor and cognitive impairment with marked choreoathetosis, self-injurious behavior and epileptic encephalopathy, to a milder phenotype[]

    Missing: Cerebellar Signs during Episodes
  • Early Infantile Epileptic Encephalopathy Type 6

    Disease onset occurs in the first year of life, followed by developmental delay with cognitive and behavioral dysfunction and substantially elevated risk of premature death[] delay or cognitive outcome did not differ between both groups.[] delay, or cognitive outcome.[]

    Missing: Cerebellar Signs during Episodes
  • Amish Lethal Microcephaly

    developmental delays; short heights; and skeletal abnormalities.Lifespan is average in length, though.[] […] limb paralysis), dysarthria (leads to difficulty in speaking), and pseudobulbar palsy (inability to control facial movements); distal amyotrophy (muscle atrophy); motor and cognitive[]

    Missing: Cerebellar Signs during Episodes
  • Mitochondrial Trifunctional Protein Deficiency

    Development (general) In children who have delayed development due to metabolic crises, management should include developmental therapies for cognitive and motor issues.[] Specialty Collaborations & Other Services Developmental - Behavioral Pediatrics (see Services below for local providers) Referral may be helpful to clarify developmental delays[]

    Missing: Cerebellar Signs during Episodes
  • Muscular Dystrophy-Dystroglycanopathy Type C9

    الصفحة 382 - All Nature is but art, unknown to thee All chance, direction, which thou canst not see; All discord, harmony not understood; All partial evil, universal good: And, spite of pride, in erring reason's spite, One truth is clear, Whatever is, is right. ‏ الصفحة 40 - Rudnicki, MA, Braun, T., Hinuma, S. and[…][]

    Missing: Cerebellar Signs during Episodes
  • Autosomal Recessive Spinocerebellar Ataxia 18

    […] with Opitz/BBB syndrome are also characterized by developmental delay, ataxia, and midline abnormalities, including hypertelorism, cleft lip/palate, esophagolaryngotracheal[] Screening for OPHN1 mutations in a large cohort of boys with cognitive impairment and vermis hypoplasia led to identification of mutations of this gene in 12%. 42 Patients[]

    Missing: Cerebellar Signs during Episodes

Further symptoms