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ετυμολογία

Vogt"s disease - 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

Vogt's disease

‎ داءُ فوغت,مُتَلاَزِمَةُ الجِسْمِ المُخَطَّط‎

Vogt's disease

داءُ فوغت

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)

Ορισμός

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.

Εμφάνιση περισσότερων ορισμών

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.

https://en.wikipedia.org/wiki/Batten disease