User Posts: Dr. Reem Saadeh Haddad, MD - Clinical Genetics, Genomics, Cytogenetics, Biochemical Genetics Specialist
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Autosomal Recessive Limb-Girdle Muscular Dystrophy Caused by Mutation in POMT2
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POMT2-related limb-girdle muscular dystrophy is a rare, inherited muscle disease. It weakens the muscles around the hips and shoulders first (the “limb-girdle” ...

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Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2N (LGMD2N)
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Autosomal recessive limb-girdle muscular dystrophy type 2N is a rare, inherited muscle disease caused by harmful changes in a gene called FKRP (fukutin-related ...

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Fukutin-Related Limb-Girdle Muscular Dystrophy
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Fukutin-related limb-girdle muscular dystrophy is a genetic muscle disease in which weakness mainly starts around the hips and shoulders (the “limb girdles”). ...

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Autosomal-Recessive Limb-Girdle Muscular Dystrophy Caused by Mutation in the FKTN Gene
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Autosomal-recessive limb-girdle muscular dystrophy caused by mutation in the FKTN gene is a genetic muscle disease. It weakens the muscles around the hips and ...

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Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2M (LGMD2M)
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Autosomal recessive limb-girdle muscular dystrophy type 2M (LGMD2M) is a rare, inherited muscle disease caused by mutations in the FKTN gene (fukutin). Fukutin ...

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Autosomal Recessive Limb-Girdle Muscular Dystrophy Caused by ANO5 Mutation
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Autosomal recessive limb-girdle muscular dystrophy caused by ANO5 mutation  is a genetic muscle disease. It happens when a person inherits two faulty copies of ...

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Anoctamin-5–Related Limb-Girdle Muscular Dystrophy R12 (LGMDR12)
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Anoctamin-5–related limb-girdle muscular dystrophy R12 (LGMDR12) is a genetic muscle disease. It happens when a person inherits two faulty copies of a gene ...

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ANO5-Related Limb-Girdle Muscular Dystrophy
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ANO5-related limb-girdle muscular dystrophy is a genetic muscle disease. It happens when a person inherits two faulty copies of the ANO5 gene (one from each ...

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Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2L (LGMD2L)
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Autosomal recessive limb-girdle muscular dystrophy type 2L (LGMD2L) is a genetic muscle disease that mainly weakens the muscles around the hips and shoulders ...

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Muscular Dystrophy-Dystroglycanopathy (Limb-Girdle) Type C1
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Muscular Dystrophy-Dystroglycanopathy (Limb-Girdle) Type C1 is a genetic muscle disease. It mainly weakens the muscles around the hips and shoulders (the ...

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Limb-Girdle Muscular Dystrophy with Intellectual Disability Syndrome (LGMD-ID)
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Limb-Girdle Muscular Dystrophy with Intellectual Disability Syndrome (LGMD-ID) is a rare, inherited muscle disease that mainly weakens the hip and shoulder ...

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Autosomal-Recessive Limb-Girdle Muscular Dystrophy Caused by Mutation in POMT1
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Autosomal-Recessive Limb-Girdle Muscular Dystrophy Caused by Mutation in POMT1 is a genetic muscle disease. It weakens the muscles around the hips and ...

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Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2K (LGMD2K)
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LGMD2K is a rare inherited muscle disease. It mainly weakens the large muscles around the hips and shoulders (the “limb-girdle” muscles). The weakness usually ...

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Pedophilia
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Pedophilia is a mental health condition in which a person has recurrent, intense sexual thoughts, urges, or fantasies about prepubescent children (children who ...

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Titin-Related Limb-Girdle Muscular Dystrophy R10 (LGMDR10, TTN-related)
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Titin-Related Limb-Girdle Muscular Dystrophy R10 (LGMDR10, TTN-related) is a rare, inherited muscle disease. It mainly weakens the large muscles around the ...

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Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2J (LGMD2J)
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Autosomal recessive limb-girdle muscular dystrophy type 2J (LGMD2J) is a genetic muscle-wasting disease caused by mutations in the TTN gene, which makes titin, ...

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Dystroglycanopathy
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Dystroglycanopathy is a group of inherited muscle diseases that happen because a key muscle-cell protein called alpha-dystroglycan (α-DG) is not properly ...

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Muscular Dystrophy-Dystroglycanopathy (Limb-Girdle) Type C5
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Muscular dystrophy-dystroglycanopathy (limb-girdle) type C5 is a genetic muscle disease caused by harmful changes (mutations) in a gene called FKRP ...

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Limb-Girdle Muscular Dystrophy Due to Fukutin-Related Protein (FKRP) Deficiency
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FKRP-related limb-girdle muscular dystrophy is a genetic muscle disease. A person inherits two faulty copies of the FKRP gene. Because of this, a protein ...

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FKRP-Related Limb-Girdle Muscular Dystrophy R9
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FKRP-related limb-girdle muscular dystrophy R9 is a genetic muscle disease. It is caused by harmful changes (variants) in a gene called FKRP. This gene makes ...

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