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1,057 Possible Causes for psychomotor disorders

  • Dementia

    (disinhibition, elation and depressive symptoms); a cluster with predominantly psychomotor symptoms (aberrant motor behaviour) and a cluster with predominantly instinctual[doi.org] […] reports four behavioural syndromes: a cluster with predominantly psychotic symptoms (hallucinations, irritability, agitation and anxiety); a cluster with predominantly mood disorders[doi.org]

  • Endocrine Dysfunction

    Clinically, compared to younger patients, the manifestations of endocrine disorders in older persons are often atypical (e.g., apathy, depression, psychomotor retardation,[endocrinenews.endocrine.org]

  • Psychomotor Retardation

    BACKGROUND: Children with developmental disorders and/or psychomotor delay may respond differently to strabismus surgery than children who develop normally, but the literature[ncbi.nlm.nih.gov] Cortico-cortical white matter motor pathway microstructure is related to psychomotor retardation in major depressive disorder.[orca.cf.ac.uk] Inflammatory markers are associated with decreased psychomotor speed in patients with major depressive disorder.[psychiatryadvisor.com]

  • 6-Pyruvoyl-Tetrahydropterin Synthase Deficiency

    The principal symptoms include psychomotor retardation, tonus disorders, convulsions, drowsiness, irritability, abnormal movements, hyperthermia, hypersalivation and difficulty[orpha.net]

  • 3-Phosphoglycerate Dehydrogenase Deficiency

    Abstract 3-phosphoglycerate dehydrogenase (PHGDH) deficiency is a disorder of L-serine biosynthesis that is characterized by congenital microcephaly, psychomotor retardation[ncbi.nlm.nih.gov] Abstract 3-phosphoglycerate-dehydrogenase (3-PGDH) deficiency is an L-serine biosynthesis disorder, characterised by congenital microcephaly, severe psychomotor retardation[ncbi.nlm.nih.gov] Abstract Congenital microcephaly, intractable seizures and severe psychomotor retardation characterize 3-phosphoglycerate dehydrogenase (3-PGDH) deficiency, a disorder of[ncbi.nlm.nih.gov]

  • Agitated Depression

    Abstract The classification of agitated depression (major depressive episode (MDE) plus psychomotor agitation) in mood disorders is unclear.[ncbi.nlm.nih.gov] disorder 精神運動性激越 psychomotor agitation 行動および行動メカニズム behavior and behavior mechanism 神経行動学的症状 neurobehavioral manifestation 精神運動障害 psychomotor disorder 精神運動性激越 psychomotor[lsd-project.jp] And it can be seen in people with bipolar disorder. But, psychomotor agitation can also be seen in major depressive disorder.[healthline.com]

  • Kohlschütter-Tönz Syndrome

    Kohlschütter-Tönz syndrome is a rare genetic disorder with epilepsy, psychomotor regression, and a severe enamel defect with yellow or brownish discoloration of the teeth.[ncbi.nlm.nih.gov] Kohlschütter-Tönz syndrome (KTS) is a rare autosomal recessive disorder characterized by amelogenesis imperfecta, psychomotor delay or regression and seizures starting early[ncbi.nlm.nih.gov]

  • Infantile 3-Phosphoglycerate Dehydrogenase Deficiency

    Disorders; Seizures 摘要 Serine biosynthesis defects can present in a broad phenotypic spectrum ranging from Neu-Laxova syndrome, a lethal disease with multiple congenital[paper.medlive.cn] Disorders Seizures Serine Young Adult Pub Type(s) Case Reports Journal Article Language eng PubMed ID 28135894 TY - JOUR T1 - Infantile Serine Biosynthesis Defect Due to[wwww.unboundmedicine.com] It is typically characterized by congenital microcephaly, intractable seizures of infantile onset, and severe psychomotor retardation.[thieme-connect.com]

  • Severe X-linked Mitochondrial Encephalomyopathy

    Definition A mitochondrial disease resulting in a neurodegenerative disorder characterized by psychomotor delay, hypotonia, areflexia, muscle weakness and wasting.[uniprot.org] UniProtKB/Swiss-Prot : 75 Combined oxidative phosphorylation deficiency 6: A mitochondrial disease resulting in a neurodegenerative disorder characterized by psychomotor delay[malacards.org] Main clinical features early-onset neurodegenerative disorder associated with dysfunction of the mitochondrial respiratory chain psychomotor delay, decreased spontaneous movement[genatlas.medecine.univ-paris5.fr]

  • Infantile Neuroaxonal Dystrophy

    INAD is a severe progressive psychomotor disorder characterized by the presence of axonal spheroids throughout the central and peripheral nervous system.[ncbi.nlm.nih.gov] Infantile neuroaxonal dystrophy, INAD, is a severe progressive psychomotor disorder with infantile onset and characterized by the presence of axonal spheroids throughout the[ncbi.nlm.nih.gov] Abstract Infantile neuroaxonal dystrophy (INAD) is a rare neurodegenerative disorder characterized by infantile onset and rapid progression of psychomotor regression and hypotonia[ncbi.nlm.nih.gov]

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