Vogt Spielmeyer disease - traducción al árabe
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Vogt Spielmeyer disease - traducción al árabe

EXTREMELY RARE AND FATAL AUTOSOMAL RECESSIVE NEURODEGENERATIVE DISORDER IN HUMANS
Batten Disease; Spielmeyer-Vogt disease; Batten's Disease; Batten-Mayou syndrome; Spielmeyer–Vogt disease; Batten mayou; Stock-Spielmeyer-Vogt syndrome; Vogt-Spielmeyer syndrome; Betten-Mayous syndrome; Spielmeyer-Sjogren; Batten's disease; Batten-Mayou disease; Spielmeyer-Vogt-Sjögren-Batten disease; Vogt-Spielmeyer disease; Spielmeyer-Vogt
  • Pickering]], Ontario, Canada, dedicated to the children who have lost or will lose their lives to Batten disease

Vogt Spielmeyer disease      
‎ داءُ فوغت شبِيلماير,الشُّحامُ السفينْغولِي الدِّمَاغِيّ اليَفَعِيّ‎
Vogt-Spielmeyer disease         
داءُ فوغت شبِيلماير
Spielmeyer-Vogt disease         
داءُ شبِيلماير - فُوغْت

Definición

Bright's disease
·- An affection of the kidneys, usually inflammatory in character, and distinguished by the occurrence of albumin and renal casts in the urine. Several varieties of Bright's disease are now recognized, differing in the part of the kidney involved, and in the intensity and course of the morbid process.

Wikipedia

Batten disease

Batten disease is a fatal disease of the nervous system that typically begins in childhood. Onset of symptoms is usually between 5 and 10 years of age. Often, it is autosomal recessive. It is the common name for a group of disorders called the neuronal ceroid lipofuscinoses (NCLs).

Although Batten disease is usually regarded as the juvenile form of NCL (or "type 3"), some physicians use the term Batten disease to describe all forms of NCL. Historically, the NCLs were classified by age of disease onset as infantile NCL (INCL), late infantile NCL (LINCL), juvenile NCL (JNCL) or adult NCL (ANCL). At least 20 genes have been identified in association with Batten disease, but juvenile NCL, the most prevalent form of Batten disease, has been linked to mutations in Battenin, the CLN3 gene. It was first described in 1903.