Early onset adhalinopathy (LGMD2D) mimicking congenital muscular dystrophy;Adhalinopatía primaria (LGMD2D) de inicio en los primeros meses de la vida que simula una distrofia muscular congénita

Revista de Neurologia

Volumn 32, Issue 7, 2001, Pages 631-635

  Castro Gago, M ^a  

^a University Hospital of Santiago de Compostela   (Spain)

Author keywords

Alpha sarcoglycanopathy; Congenital muscular dystrophy; Dystrophinopathy; Progressive muscular dystrophy; Sarcoglycanopathy

Indexed keywords

BIOLOGICAL MARKER;

ARTICLE; BIOPSY; CASE REPORT; CHILD; GENETICS; HUMAN; INFANT; LIMB GIRDLE MUSCULAR DYSTROPHY; MALE; MUTATION; PATHOLOGY; PATHOPHYSIOLOGY; PRESCHOOL CHILD; SKELETAL MUSCLE;

BIOLOGICAL MARKERS; BIOPSY; CHILD; CHILD, PRESCHOOL; HUMANS; INFANT; MALE; MUSCLE, SKELETAL; MUSCULAR DYSTROPHIES, LIMB-GIRDLE; MUTATION;

EID: 0037477998     PISSN: 02100010     EISSN: None     Source Type: Journal    
DOI: 10.33588/rn.3207.2000511     Document Type: Article

References (3)

1. Walton JN, Nattras FJ. On the classification, natural history and treatment of the myopathies. Brain 1954; 77: 169-231.
2. Dubowitz V. Muscle disorders in childhood. 2 ed. London: WB Saunders; 1995.
3. Dubowitz V. Progressive muscular dystrophy of the Duchenne type in females and its mode of inheritance. Brain 1960; 83: 432-9.