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In questa pagina puoi ottenere un'analisi dettagliata di una parola o frase, prodotta utilizzando la migliore tecnologia di intelligenza artificiale fino ad oggi:
- come viene usata la parola
- frequenza di utilizzo
- è usato più spesso nel discorso orale o scritto
- opzioni di traduzione delle parole
- esempi di utilizzo (varie frasi con traduzione)
- etimologia
Cosa (chi) è X-linked sideroblastic anemia and spinocerebellar ataxia - definizione
X-linked sideroblastic anemia and spinocerebellar ataxia
HUMAN DISEASE
X-linked sideroblastic anemia and spinocerebellar ataxia is a very rare genetic disorder which is characterized by mild sideroblastic anemia, and spinocerebellar ataxia that either doesn't progress or does so very slowly. Additional findings include dysarthria, tremors and eye movement anomalies.
Spinocerebellar ataxia
![autosomal-dominant]] cerebellar ataxias](https://commons.wikimedia.org/wiki/Special:FilePath/Autosomal dominant - en.svg?width=200 "autosomal-dominant]] cerebellar ataxias")
![autosomal recessive]] disorders in which ataxia is a prominent feature](https://commons.wikimedia.org/wiki/Special:FilePath/autorecessive.svg?width=200 "autosomal recessive]] disorders in which ataxia is a prominent feature")
GROUP OF DOMINANTLY INHERITED, PREDOMINATELY LATE-ONSET, CEREBELLAR ATAXIAS. NEURO-DEVELOPMENTAL OUTCOME AND BRAIN-DERIVED NEUROTROPHIC FACTOR LEVEL IN RELATION TO FEEDING PRACTICE IN EARLY INFANCY.
Spinocerebellar ataxias; Spinocerebellar degeneration; Spinocerebellar atrophy; X-linked recessive spinocerebellar ataxia; Spino-cerebellar Ataxia; Spinocerebellar Degeneration; Spinal cerebellar atrophy; Spinocerebellar Ataxia; Spinocerebellar degenerations; Spinocerebellar ataxia 5; Spinocerebellar Atrophy
Spinocerebellar ataxia (SCA) is a progressive, degenerative, genetic disease with multiple types, each of which could be considered a neurological condition in its own right. An estimated 150,000 people in the United States have a diagnosis of spinocerebellar ataxia at any given time.
Spinocerebellar ataxia type 6
HUMAN DISEASE
SCA6; Episodic and progressive ataxia; Spinocerebellar ataxia type-6
Spinocerebellar ataxia type 6 (SCA6) is a rare, late-onset, autosomal dominant disorder, which, like other types of SCA, is characterized by dysarthria, oculomotor disorders, peripheral neuropathy, and ataxia of the gait, stance, and limbs due to cerebellar dysfunction. Unlike other types, SCA 6 is not fatal.
