Arnolone Syndrome (2024)

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Arnolone Syndrome? ›

While SOA sounded like a group and Mount Hio eruption sounded like a volcanic eruption, the Arnolone Syndrome seemed to be something quite intriguing and messed up. The truth is that the Arnolone Syndrome doesn't exist and it is something made up by mangaka Tatsuki Fujimoto to confuse his readers.

Avellis syndrome is a rare bulbar syndrome. The main lesions may involve nucleus ambiguus and the lateral spinothalamic tract. The typical reported clinical manifestations are hoarseness, dysphagia, pain, and temperature disturbance of contralateral body.

A rare X-linked syndromic intellectual disability considered to be a severe variant of dyskeratosis congenita characterized by intrauterine growth retardation, microcephaly, cerebellar hypoplasia, progressive combined immune deficiency and aplastic anemia.

Fatigue and muscle cramps are the main features; they are associated with nausea and intermittent vomiting.

Clumsy, uncoordinated movements, including difficulty with handwriting. Difficulty managing emotions, sometimes leading to verbal or behavioral outbursts, self-injurious behaviors, or tantrums. Not understanding other peoples' feelings or perspectives. Hypersensitivity to lights, sounds, and textures.

For most children, life expectancy will not be different from that of children without this syndrome. Life expectancy can be shortened due to a difficult-to-treat form of epilepsy. Children get Adults with KDM5C syndrome can have children.

Life expectancy depends on the severity of the condition and can vary from death in childhood to survival into adulthood.

The principal symptom of subjects suffering from King-Kopetzky syndrome is a perceived difficulty in recognizing and understanding speech in noisy backgrounds.

Symptoms directly related to the Kernohan's notch is most commonly paralysis or weakness on one side of the body (ipsilateral paralysis / paresis), the so-called Kernohan's sign. Paralysis and weakness is known as hemiplegia and hemiparesis, respectively.

A rare, genetic neurological disorder characterized by the presence of diffuse pachygyria and arachnoid cysts, psychom*otor developmental delay and intellectual disability. Seizures (absence, atonic and generalized tonic-clonic) and, on occasion, headache are also associated. ORPHA:2798. Synonym(s): Kuzniecky syndrome.

What is the symptoms of Schmahmann's syndrome? ›

The syndrome was characterized by four clusters of symptoms including: (a) impairment of executive functions such as planning, set-shifting, verbal fluency, abstract reasoning and working memory, (b) impaired visuo-spatial cognition, (c) personality changes with blunting of affect or abnormal behaviour, and (d) ...

The symptoms typically include vertigo, diplopia, dysarthria, Horner's syndrome, and numbness on one side of the face and the opposite limb [4]. However, there are subtypes of lateral medullary syndromes such as Opalski syndrome which present with unique and atypical symptoms.

Kohlschutter-Tonz syndrome (KTZS) is an autosomal recessive disorder characterized by severe global developmental delay, early-onset intractable seizures, spasticity, and amelogenesis imperfecta affecting both primary and secondary teeth and causing yellow or brown discoloration of the teeth.

Tay Sachs disease (TSD) is a progressive, lethal neurodegenerative disorder caused by a deficiency of enzyme hexosaminidase-A resulting in the accumulation of GM2 gangliosides. Based on the presentation age, the disease is classified into infantile, juvenile, and adult forms.

Signs and symptoms of CANOMAD may include loss of muscle, tendon, and joint sensation, abnormal gait (walk), ataxia, tingling sensation on the skin around the mouth or extremities, paralysis of eye muscles, difficulty swallowing and speaking, and rarely respiratory muscle weakness.

The onset of seizures was exclusively during early childhood. The Kaplan–Meier estimate of survival was dismal (median survival 6.5 years; 95% CI 3.6–9.4), and none of the patients survived beyond the age of 12 years.

Landau-Kleffner syndrome (LKS) is a condition that shows up during childhood, causing difficulties with speech and seizures. Children with LKS lose the ability to talk and understand speech. This loss is called aphasia. Many children with LKS also have seizures, episodes of uncontrolled body movement.

This disorder usually presents in early childhood with signs of progressively worsening eye and balance problems; significant developmental delay and intellectual disability; and characteristic skin changes. Revesz Syndrome is caused by mutations in the TRF1-Interacting Nuclear Factor 2 (TINF2) and telomeres.