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nutritional dystrophy - translation to αραβικά
INHERITED OCULAR DISORDER CHARACTERIZED BY THE LOSS OF CONE CELLS
Cone-rod dystrophy; Rod dystrophy
nutritional dystrophy
الحَثَلُ التَّغْذَوِيّ
facioscapulohumeral muscular dystrophy
![Structure]] of DUX4 protein full-length (FL), with short (S) version indicated.](https://commons.wikimedia.org/wiki/Special:FilePath/DUX4-FL Protein.png?width=200 "Structure]] of DUX4 protein full-length (FL), with short (S) version indicated.")
![Microscopic cross-sectional views of FSHD-affected [[muscle fiber]]s. Visible is inflammation and fibrosis, as well as muscle fiber shape change, death, and regeneration.](https://commons.wikimedia.org/wiki/Special:FilePath/Facioscapulohumeral muscular dystrophy histology.jpg?width=200 "Microscopic cross-sectional views of FSHD-affected [[muscle fiber]]s. Visible is inflammation and fibrosis, as well as muscle fiber shape change, death, and regeneration.")
![[[Funduscopy]] of the retinal: (A) normal blood vessels (B) tortuous blood vessels, as often seen with FSHD](https://commons.wikimedia.org/wiki/Special:FilePath/Retinal vessel tortuosity.jpg?width=200 "[[Funduscopy]] of the retinal: (A) normal blood vessels (B) tortuous blood vessels, as often seen with FSHD")
![Scapula-to-scapula scapulopexy, pre- and post-operation. The scapulas are tethered together into a retracted position with an [[Achilles tendon]] graft, which, in this case, rendered the rhomboid major muscles distinguishable.](https://commons.wikimedia.org/wiki/Special:FilePath/Before and after Scapula-to-scapula scapulopexy FSHD.png?width=200 "Scapula-to-scapula scapulopexy, pre- and post-operation. The scapulas are tethered together into a retracted position with an [[Achilles tendon]] graft, which, in this case, rendered the rhomboid major muscles distinguishable.")
MUSCULAR DYSTROPHY THAT CLASSICALLY WEAKENS THE MUSCLES OF THE FACE (FACIO), SHOULDER GIRDLE (SCAPULO) AND UPPER ARM (HUMERUS). WEAKNESS USUALLY IS ASYMMETRICAL AND DEVELOPS IN OTHER AREAS OF THE BODY AS WELL, SUCH AS THE ABDOMEN AND SHIN.
Facioscapulohumeral Muscular Dystrophy; FSHD; Facioscapulohumeral dystrophy; Muscular dystrophy, facioscapulohumeral; Landouzy-Dejerine; Landouzy-Dejerine syndrome; Erb-Landouzy-Dejerine syndrome; Landouzy-Dejerine dystrophy or atrophy; Landouzy-Dejerine dystrophy; Landouzy-Dejerine atrophy; Facioscapulohemeral MD; Facioscapulohumeral MD; Landouzy-Dejerine muscular dystrophy; FSHMD; Muscular dystrophy facioscapulohumeral; Faciohumeroscapular muscular dystrophy; Landouzy–Dejerine muscular dystrophy
الحَثَلُ العَضَلِيُّ الوَجْهِيُّ الكَتِفِيُّ العَضُدِيُّ
macular corneal dystrophy
CORNEAL DYSTROPHY THAT IS CHARACTERIZED BY CORNEAL HAZE, SEVERE PHOTOPHOBIA AT NIGHT ,GRADUAL VISION IMPAIRMENT ,BILATERAL LOSS OF VISION, EVENTUALLY NECESSITATING CORNEAL TRANSPLANTATION RESULTING FROM PROGRESSIVE PUNCTATE OPACITIES IN THE CORNEA
Groenouw Type II corneal dystrophy; Fehr corneal dystrophy; Type II Groenow's dystrophy
حَثَلُ البُقْعَةِ و القَرْنِيَّة:النمط الثاني لغرونو
Ορισμός
muscular dystrophy
Muscular dystrophy is a serious disease in which your muscles gradually weaken.
N-UNCOUNT
Βικιπαίδεια
Cone dystrophy
A cone dystrophy is an inherited ocular disorder characterized by the loss of cone cells, the photoreceptors responsible for both central and color vision.
