Clinical spectrum and diagnostic criteria of infantile spinal muscular atrophy: further delineation on the basis of SMN gene deletion findings.

Rudnik-Schöneborn, S; Forkert, R; Hahnen, E; Wirth, B; Zerres, K

Rudnik-Schöneborn, S; Forkert, R; Hahnen, E; Wirth, B; Zerres, K.

Affiliation

Rudnik-Schöneborn S; Institute for Human Genetics, University of Bonn, Germany.

Neuropediatrics ; 27(1): 8-15, 1996 Feb.

Article in En | MEDLINE | ID: mdl-8677029

Subject(s)

Spinal Muscular Atrophies of Childhood/genetics; Arthrogryposis/complications; Asphyxia Neonatorum; Bone and Bones/physiopathology; Brain/physiopathology; Child, Preschool; Chromosomes, Human, Pair 5; Female; Fractures, Bone/complications; Fractures, Bone/physiopathology; Gene Deletion; Homozygote; Humans; Infant; Infant, Newborn; Male; Olivopontocerebellar Atrophies/complications; Olivopontocerebellar Atrophies/physiopathology; Spinal Muscular Atrophies of Childhood/complications; Spinal Muscular Atrophies of Childhood/physiopathology

Search on Google

XML

PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Spinal Muscular Atrophies of Childhood Type of study: Diagnostic_studies / Prognostic_studies Limits: Child, preschool / Female / Humans / Infant / Male / Newborn Language: En Journal: Neuropediatrics Year: 1996 Type: Article Affiliation country: Germany

Search on Google

XML

PubMed Links