Vogt-Koyanagi syndrome - translation to αραβικά
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Vogt-Koyanagi syndrome - translation to αραβικά

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-Koyanagi syndrome         
MULTISYSTEM DISEASE
Vogt–Koyanagi–Harada syndrome; Vogt-Koyanagi-Harada disease; VKH; VKH syndrome; VKH disease; VKH-like disease; VKH-like syndrome; Vogt-Koyanagi-Harada-like syndrome; Uveodermatologic syndrome; Uveodermatologic disease; Uvrodermatological syndrome; Vogt-Koyanagi-Harada; Yuge's sybdrome; Harada’s disease; Harada's disease; Vogt-Koyanagi-Harada syndrome; Uveitis-vitiligo-alopecia-poliosis syndrome; Harada's syndrome; Vogt-Koyanagi syndrome; User:FeatherPluma/Vogt-Koyanagi-Harada disease; User:FeatherPluma/Vogt–Koyanagi–Harada disease; Uveomeningoencephalitic syndrome
مُتَلاَزِمَةُ فوغت-كوياناغي (أعراض عينية جلدية تصاحب التهاب السحايا)
Batten-Mayou disease         
داءُ باتن- مايو
Vogt-Spielmeyer disease         
داءُ فوغت شبِيلماير

Ορισμός

Reye's syndrome
['re?z, 'r??z]
¦ noun a life-threatening metabolic disorder in young children, of uncertain cause.
Origin
1960s: named after the Australian paediatrician Ralph D. K. Reye.

Βικιπαίδεια

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.