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2,415 Possible Causes for Hemiplegia, Lack of Developmental Milestones, Mutation in the VPS53 Gene

  • Pontocerebellar Hypoplasia Type 2E

    […] of childhood, Migraine, familial hemiplegic ATP1A3 Alternating hemiplegia of childhood CACNA1A Episodic ataxia, Migraine, familial hemiplegic KCNK18 Migraine, with or without[genda.com.ar] The disease, which the researchers have called PCCA2 (Progressive Cerebello-Cerebral Atrophy Type 2), is caused by two mutations in the VPS53 gene.[sciencedaily.com] In the case of PCCA, the families that have it may have one of two mutations in one gene called SepSecS, or one mutation in an unrelated gene, called VPS53.[popsci.com]

  • Hemiplegia

    hemiplegia NOS Infantile hemiplegia NOS (disorder) Infantile hemiplegia [Ambiguous] Postnatal infantile hemiplegia NOS Postnatal infantile hemiplegia Hemiconvulsion hemiplegia[wikidata.org] milestones.[cerebral-palsy-information.com] hemiplegia (disorder) Infantile hemiplegia NOS Infantile hemiplegia NOS (disorder) Infantile hemiplegia [Ambiguous] Postnatal infantile hemiplegia NOS Postnatal infantile[wikidata.org]

    Missing: Mutation in the VPS53 Gene
  • Epidural Hematoma

    […] movements Delays developmental milestones and motor skills Difficulty grasping and holding onto objects Muscle tone may vary, changing from extremely rigid to extremely floppy[birthinjuryguide.org] […] microangiopathic changes Arterial hypertension and increasing age are the most important risk factors Clinical features Lucid interval, then loss of consciousness Headache Hemiplegia[amboss.com] Left hemiplegia was deteted. Right fronto-parietal trephine cranitomy with evacuation of extradural haematoma was done under general anaesthesia.[neurologyindia.com]

    Missing: Mutation in the VPS53 Gene
  • Herpes Simplex Encephalitis

    She was febrile and drowsy with right sided hemiplegia and papilledema.[ncbi.nlm.nih.gov] Before the onset of illness, the patient was appropriately following her normal developmental milestones and was able to sit, stand, and walk independently.[jaoa.org] Post ictal left hemiplegia and confusion lasted for an hour.[omicsonline.org]

    Missing: Mutation in the VPS53 Gene
  • Cerebral Palsy

    For example, if a child is developmentally ready to stand and explore the environment but is limited by a lack of motor control, the use of a stander should be encouraged[emedicine.com] To assess quantitatively the effects of Neuromuscular Taping (NMT) on the upper limb in a female child with left hemiplegia, due to Cerebral Palsy (CP).[ncbi.nlm.nih.gov] KEYWORDS: diplegia; fine motor skills; finger perception; finger sensitivity; hemiplegia[ncbi.nlm.nih.gov]

    Missing: Mutation in the VPS53 Gene
  • Athetoid Cerebral Palsy

    […] and hemiparesis G81.0 Flaccid hemiplegia G81.00 …… affecting unspecified side G81.01 …… affecting right dominant side G81.02 …… affecting left dominant side G81.03 …… affecting[icd10data.com] Other common symptoms noted include: Parents can monitor whether their children are meeting expected developmental milestones.[cerebralpalsygroup.com] Spastic hemiplegia – patients experience problems controlling movement on one side of the body. Spastic monoplegia – patients lack muscle control in one arm or one leg.[legalseeker.com]

    Missing: Mutation in the VPS53 Gene
  • Stroke

    Specifically, this exploratory study investigates changes in gait pattern among stroke patients with hemiparesis or hemiplegia during gait recovery.[ncbi.nlm.nih.gov] This case report presents the clinical record of a 37-year-old man who presented with a dense right hemiplegia, found to be caused by a left medial medullary stroke.[ncbi.nlm.nih.gov] Effects of a right hemisphere stroke: The effects of a right hemisphere stroke may include the following: left-sided weakness (left hemiparesis) or paralysis (left hemiplegia[web.archive.org]

    Missing: Lack of Developmental Milestones Mutation in the VPS53 Gene
  • Polyneuropathy

    Episodic ataxia and hemiplegia caused by the 8993T- C mitochondrial DNA mutation. J Med Genet. 2007 Dec;44(12):797-9.[disorders.eyes.arizona.edu] References Article Title: Episodic ataxia and hemiplegia caused by the 8993T- C mitochondrial DNA mutation Craig K, Elliott HR, Keers SM, Lambert C, Pyle A, Graves TD, Woodward[disorders.eyes.arizona.edu]

    Missing: Lack of Developmental Milestones Mutation in the VPS53 Gene
  • Cerebral Thrombosis

    Hemiplegia then cerebral thrombosis I have just received a death certificate which gives the cause of death as: 1(a) Hemiplegia (which she had had for 15 days) 1(b) cerebral[british-genealogy.com] Thrombosis, brain) 434.0 Encephalomalacia (brain) (cerebellar) (cerebral) (cerebrospinal) (see also Softening, brain) 348.89 thrombotic (see also Thrombosis, brain) 434.0 Hemiplegia[icd9data.com] METHOD: 180 patients with hemiplegia due to cerebral thrombosis were randomly divided into 2 groups: the treatment group (treated with scalp acupuncture by using the lifting[ncbi.nlm.nih.gov]

    Missing: Lack of Developmental Milestones Mutation in the VPS53 Gene
  • Ataxic Cerebral Palsy

    Spastic cerebral palsy may manifest in a few different ways, including: Hemiplegia – The muscles on one side of the body are affected. Diplegia – Both legs are affected.[birthinjurycenter.com] It may be noticed that developmental milestones such as smiling and rolling over are delayed or not reached. As a child develops, other symptoms may appear.[southerncross.co.nz] Hemiplegia means one side of the body is affected, diplegia is where two limbs are affected, monoplegia where one limb is affected and quadriplegia means all four limbs (and[nhs.uk]

    Missing: Mutation in the VPS53 Gene

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