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133 Possible Causes for MRI Shows Increased Connective Tissue and Fat, Mutation in the DNAJB6 Gene, Onset of Symptoms in First or Second Decade of Life

  • Limb-Girdle Muscular Dystrophy Type 2L

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] LGMD1E (note that some references call this LGMD1D) is caused by a mutation on chromosome 7 in the DNAJB6 gene (DNAJ/HSP40 Homolog, subfamily B, Member 6).[emedicine.medscape.com] Aggregates contain DNAJB6, TDP-43, and SMI-31 LGMD1F is caused by a mutation on chromosome 7 in the transportin 3 ( TNPO3 ) gene. [54] Transportin 3 is a member of the importinb[emedicine.medscape.com]

  • Limb-Girdle Muscular Dystrophy Type 1E

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] LGMD1E (note that some references call this LGMD1D) is caused by a mutation on chromosome 7 in the DNAJB6 gene (DNAJ/HSP40 Homolog, subfamily B, Member 6).[emedicine.medscape.com] Aggregates contain DNAJB6, TDP-43, and SMI-31 LGMD1F is caused by a mutation on chromosome 7 in the transportin 3 ( TNPO3 ) gene. [54] Transportin 3 is a member of the importinb[emedicine.medscape.com]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Limb-Girdle Muscular Dystrophy

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] DNAJB6 is the causative gene for limb-girdle muscular dystrophy 1D (LGMD1D).[ncbi.nlm.nih.gov] Phe93Leu mutation based on a targeted gene analysis.[ncbi.nlm.nih.gov]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Emery-Dreifuss Muscular Dystrophy Type 2

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] LGMDID is caused by heterozygous missense mutations in the DNAJB6 gene at chr. 7q36.3 (10).[archive.org] LGMD1D is caused by heterozygous missense mutations in the DNAJB6 gene at chr. 7q36.3 (10).[docksci.com]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Limb-Girdle Muscular Dystrophy Type 2J

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] LGMD1E (note that some references call this LGMD1D) is caused by a mutation on chromosome 7 in the DNAJB6 gene (DNAJ/HSP40 Homolog, subfamily B, Member 6).[emedicine.medscape.com] Aggregates contain DNAJB6, TDP-43, and SMI-31 LGMD1F is caused by a mutation on chromosome 7 in the transportin 3 ( TNPO3 ) gene. [54] Transportin 3 is a member of the importinb[emedicine.medscape.com]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Limb-Girdle Muscular Dystrophy Type 2E

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] LGMD1E (note that some references call this LGMD1D) is caused by a mutation on chromosome 7 in the DNAJB6 gene (DNAJ/HSP40 Homolog, subfamily B, Member 6).[emedicine.medscape.com] Aggregates contain DNAJB6, TDP-43, and SMI-31 LGMD1F is caused by a mutation on chromosome 7 in the transportin 3 ( TNPO3 ) gene. [54] Transportin 3 is a member of the importinb[emedicine.medscape.com]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Limb-Girdle Muscular Dystrophy Type 2F

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] LGMD1E (note that some references call this LGMD1D) is caused by a mutation on chromosome 7 in the DNAJB6 gene (DNAJ/HSP40 Homolog, subfamily B, Member 6).[emedicine.medscape.com] Aggregates contain DNAJB6, TDP-43, and SMI-31 LGMD1F is caused by a mutation on chromosome 7 in the transportin 3 ( TNPO3 ) gene. [54] Transportin 3 is a member of the importinb[emedicine.medscape.com]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Muscular Dystrophy-Dystroglycanopathy Type C5

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] LGMD1E (note that some references call this LGMD1D) is caused by a mutation on chromosome 7 in the DNAJB6 gene (DNAJ/HSP40 Homolog, subfamily B, Member 6).[emedicine.medscape.com] Aggregates contain DNAJB6, TDP-43, and SMI-31 LGMD1F is caused by a mutation on chromosome 7 in the transportin 3 ( TNPO3 ) gene. [54] Transportin 3 is a member of the importinb[emedicine.medscape.com]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Limb-Girdle Muscular Dystrophy Type 2Q

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] LGMD1E (note that some references call this LGMD1D) is caused by a mutation on chromosome 7 in the DNAJB6 gene (DNAJ/HSP40 Homolog, subfamily B, Member 6).[emedicine.medscape.com] Aggregates contain DNAJB6, TDP-43, and SMI-31 LGMD1F is caused by a mutation on chromosome 7 in the transportin 3 ( TNPO3 ) gene. [54] Transportin 3 is a member of the importinb[emedicine.medscape.com]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Muscular Dystrophy-Dystroglycanopathy Type C3

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] LGMD1E (note that some references call this LGMD1D) is caused by a mutation on chromosome 7 in the DNAJB6 gene (DNAJ/HSP40 Homolog, subfamily B, Member 6).[emedicine.medscape.com] Aggregates contain DNAJB6, TDP-43, and SMI-31 LGMD1F is caused by a mutation on chromosome 7 in the transportin 3 ( TNPO3 ) gene. [54] Transportin 3 is a member of the importinb[emedicine.medscape.com]

    Missing: MRI Shows Increased Connective Tissue and Fat