Viewing Study NCT01403402


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Ignite Modification Date: 2026-03-02 @ 11:10 PM
Study NCT ID: NCT01403402
Status: RECRUITING
Last Update Posted: 2021-08-09
First Post: 2011-07-26
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Congenital Muscle Disease Study of Patient and Family Reported Medical Information
Sponsor: Cure CMD
Organization:

Conditions & Keywords Data

Conditions:

Conditions

Condition Brief Condition Text View
None Congenital Muscular Dystrophy With ITGA7 (Integrin Alpha-7) Deficiency View
None Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy and Abnormal Glycosylation of Dystroglycan With … View
None Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Fatty Liver and Infantile-onset Cataract … View
None Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Hypoglycosylation of Dystroglycan) View
None Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Hypoglycosylation of Dystroglycan and Epilepsy) View
None Alpha-Dystroglycanopathy (Dystroglycanopathy, Congenital With or Without Mental Retardation (Formerly MDC1C)) View
None Alpha-Dystroglycanopathy (Fukuyama CMD) View
None Alpha-Dystroglycanopathy (LGMDR09 FKRP Related (Formerly LGMD2I)) View
None Alpha-Dystroglycanopathy (LGMDR11 POMT1 Related (Formerly LGMD2K)) View
None Alpha-Dystroglycanopathy (LGMDR13 FKTN Related (Formerly LGMD2M)) View
None Alpha-Dystroglycanopathy (LGMDR14 POMT2 Related (Formerly LGMD2N)) View
None Alpha-Dystroglycanopathy (LGMDR15 POMGnT1 Related (Formerly LGMD2O)) View
None Alpha-Dystroglycanopathy (LGMDR19 GMPPB Related (Formerly LGMD2T)) View
None Alpha-Dystroglycanopathy (LGMDR20 ISPD Related (Formerly LGMD2U)) View
None Alpha-Dystroglycanopathy (LGMDR24 POMGnT2 Related) View
None Alpha-Dystroglycanopathy (Muscle Eye Brain Disease (MEB)) View
None Alpha-Dystroglycanopathy (Walker Warburg Syndrome (WWS)) View
None Choline Kinase B Receptor - CHKB View
None Collagen VI Related Disorders View
None Collagen XII Related Disorders View
None Congenital Muscular Dystrophy Not Otherwise Specified (Including Merosin Positive) View
None Congenital Muscular Dystrophy With Cataracts and Intellectual Disability (MDCCAID) View
None Congenital Muscular Dystrophy With Joint Hyperlaxity View
None Congenital Muscular Dystrophy With Rigid Spine Related to ACTA1 View
None Emery-Dreifuss Muscular Dystrophy View
None GOLGA2-related Congenital Muscle Dystrophy With Brain Involvement View
None LMNA Related Disorders View
None Merosin Deficient CMD (Full or Partial) View
None Nesprin Related MD (SYNE1) View
None SELENON Related Disorders (Previously Known as SEPN1) View
None SELENON Related Myopathy (Aka SEPN1) View
None Telethonin CMD View
None Congenital Myasthenic Syndrome View
None Limb-Girdle Muscular Dystrophy View
None LGMDD01 - DNAJB6 (Formerly LGMD1D) View
None LGMDD05 - Collagen VI Related Bethlem Myopathy (Dominant) View
None LGMDR07 - Telethonin (TCAP) Related (Formerly LGMD2G) View
None LGMDR08 - TRIM Related (Formerly LGMD2H) View
None LGMDR09 - FKRP Related (Formerly LGMD2I) View
None LGMDR10 - Titin (TTN) Related (Formerly LGMD2J) View
None LGMDR11 - POMT1 Related (Formerly LGMD2K) View
None LGMDR13 - Fukutin (FKTN) Related (Formerly LGMD2M) View
None LGMDR14 - POMT2 Related (Formerly LGMD2N) View
None LGMDR15 - POMGnT1 Related (Formerly LGMD2O) View
None LGMDR16 - DAG1 Related Dystroglycanopathy (Formerly LGMD2P) View
None LGMDR17 - Plectin (PLEC) Related (Formerly LGMD2Q) View
None LGMDR18 - TRAPPC11 Related (Formerly LGMD2S) View
None LGMDR19 - GMPPB Related (Formerly LGMD2T) View
None LGMDR20 - ISPD Related (Formerly LGMD2U) View
None LGMDR22 - Collagen VI Related Bethlem Myopathy (Recessive) View
None LGMDR23 - LAMA2 Related View
None LGMDR24 - POMGnT2 Related View
Keywords:

Keywords

Keyword Brief Keyword Text View
None Congenital Muscular Dystrophy View
None Congenital Myopathy View
None Neuromuscular Diseases View
None Musculoskeletal Diseases View