hypophyseal dystrophy - traduction vers arabe
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hypophyseal dystrophy - traduction vers arabe

INHERITED OCULAR DISORDER CHARACTERIZED BY THE LOSS OF CONE CELLS
Cone-rod dystrophy; Rod dystrophy

hypophyseal dystrophy      
‎ الحَثَلُ النُّخامِيّ‎
pituitary portal system         
SYSTEM OF BLOOD VESSELS
Pituitary portal system; Hypothalamo-hypophyseal portal system; Hypothalamo-hypophyseal system; Hypothalamic-hypophyseal portal system; Hypothalamohypophysial; Hypothalamo-hypophysial portal circulation; Hypophyseal circulation; Hypothalamo-pituitary portal system; Venae portales hypophysiales; Hypophyseal portal circulation; Hypophyseal portal systems
‎ الجَهازُ النَّخامِيُّ البَوَّابيّ, الجُمْلَةُ البابِيَّةُ النُّخامِيَّة‎
facioscapulohumeral muscular dystrophy         
  • }
  • Structure]] of DUX4 protein full-length (FL), with short (S) version indicated.
  • 400px
  • American Academy of Neurology (ANN) guidelines for genetic testing for suspected FSHD. Not all laboratories follow this workflow.
  • MRI showing asymmetrical involvement of various muscles in FSHD
  • Diagram showing restriction enzyme sites used to differentiate between D4Z4 repeat arrays of 4q and 10q.
  • D4Z4 array examples, with each D4Z4 repeat represented by a triangle. The circles above the triangles represent DNA methylation, which determine DNA packaging as represented by the circles in line with the triangles.
  • Bilateral scapular winging, right moreso than left. Left image showing wall push test, right image showing attempted shoulder flexion.
  • 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.
  • right
  • [[Funduscopy]] of the retinal: (A) normal blood vessels (B) tortuous blood vessels, as often seen with FSHD
  • pages=5901–14}}</ref>
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

Définition

muscular dystrophy
Muscular dystrophy is a serious disease in which your muscles gradually weaken.
N-UNCOUNT

Wikipédia

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.