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26 Possible Causes for Onset of Symptoms in First or Second Decade of Life, Syndactyly 2/3

  • Cardiodysrhythmic Potassium-Sensitive Periodic Paralysis

    Figure (A) Fifth digit clinodactyly and (B) syndactyly of the toes 2 and 3, highly suggestive of Andersen-Tawil syndrome.[scielo.br] […] of signs and symptoms typically beginning in the first or second decade of life (Table 1 ).[doi.org] […] of toes 2 and 3 B.[ncbi.nlm.nih.gov]

  • Young Adult-Onset Distal Hereditary Motor Neuropathy

    Spinocerebellar ataxia type 26 Spinocerebellar ataxia type 28 Syndactyly type 3 Syndromic multisystem autoimmune disease due to Itch deficiency Thiamine-responsive maple syrup[csbg.cnb.csic.es] Age of onset is in the second and third decades of life and rarely in the first. Recovery is usually complete and begins weeks to months after the onset of symptoms.[emedicine.medscape.com] […] type 3 Spastic paraplegia 31 Wrinkly skin syndrome Congenital pseudoarthrosis SHORT syndrome Deafness conductive ptosis skeletal anomalies Juvenile retinoschisis Deafness[checkrare.com]

  • Limb-Girdle Muscular Dystrophy Type 1E

    […] type 1 Syndactyly type 2 Syndactyly type 3 Syndactyly type 4 Syndactyly type 5 Syndactyly type 6 Syndactyly type 8 Syndactyly-camptodactyly and clinodactyly of fifth fingers-bifid[se-atlas.de] 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] Subependymal nodular heterotopia Sucking/swallowing disorder Summitt syndrome Symbrachydactyly of hands and feet Symphalangism with multiple anomalies of hands and feet Syndactyly[se-atlas.de]

  • Muscular Dystrophy-Dystroglycanopathy Type C9

    […] type 1 Syndactyly type 2 Syndactyly type 3 Syndactyly type 4 Syndactyly type 5 Syndactyly type 6 Syndactyly type 8 Syndactyly-camptodactyly and clinodactyly of fifth fingers-bifid[se-atlas.de] 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] Subependymal nodular heterotopia Sucking/swallowing disorder Summitt syndrome Symbrachydactyly of hands and feet Symphalangism with multiple anomalies of hands and feet Syndactyly[se-atlas.de]

  • Secondary Myopathy

    […] of toes 2 and 3 One of the above 3 in addition to at least 1 other family member who meets 2 of the 3 criteria.[sites.google.com] Childhood onset weakness, contractures, and early cardiac involvement. Symptoms usually develop in the first or second decade of life.[sites.google.com] Characteristic facies, dental anomalies, small hands and feet, and at least 2 of the following: Low-set ears Widely spaced eyes Small mandible Fifth-digit clinodactyly Syndactyly[sites.google.com]

  • Muscular Dystrophy-Dystroglycanopathy Type C2

    […] type 1 Syndactyly type 2 Syndactyly type 3 Syndactyly type 4 Syndactyly type 5 Syndactyly type 6 Syndactyly type 8 Syndactyly-camptodactyly and clinodactyly of fifth fingers-bifid[se-atlas.de] 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] Subependymal nodular heterotopia Sucking/swallowing disorder Summitt syndrome Symbrachydactyly of hands and feet Symphalangism with multiple anomalies of hands and feet Syndactyly[se-atlas.de]

  • Emery-Dreifuss Muscular Dystrophy Type 2

    Atrophy 1 Symphalangism, Proximal, 1B 1 Syndactyly Cenani Lenz Type 3 Syndactyly Type 5 1 Syndactyly, Mesoaxial Synostotic, with Phalangeal Reduction 2 Synpolydactyly 1 2[preventiongenetics.com] 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] Surfactant Metabolism Dysfunction, Pulmonary, 2 3 Surfactant Metabolism Dysfunction, Pulmonary, 3 3 Surfactant Metabolism Dysfunction, Pulmonary, 5 2 Sveinsson Chorioretinal[preventiongenetics.com]

  • Distal Myopathy Type 3

    […] of toes 2 and 3 One of the above 3 in addition to at least 1 other family member who meets 2 of the 3 criteria.[sites.google.com] 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] Characteristic facies, dental anomalies, small hands and feet, and at least 2 of the following: Low-set ears Widely spaced eyes Small mandible Fifth-digit clinodactyly Syndactyly[sites.google.com]

  • Congenital Merosin-Positive Muscular Dystrophy

    3 toe Syndactyly CNS malformation Behavioral phenotype Assay of 7 dehydrocholesterol Levels in plasma Congenital disorders of Glycosylation (CDG) AR Defect in N-glyosylation[mafiadoc.com] 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] […] calcifications Elevated levels of Plasma VLCFA Smith Lemli–Opitz syndrome MIM #270400 AR Deficiency of 7-dehydrocholesterol reductase Dysmorphic facies Midline defects Hypotonia 2-[mafiadoc.com]

  • Polyglucosan Body Myopathy Type 2

    […] of toes 2 and 3 One of the above 3 in addition to at least 1 other family member who meets 2 of the 3 criteria.[sites.google.com] Childhood onset weakness, contractures, and early cardiac involvement. Symptoms usually develop in the first or second decade of life.[sites.google.com] Characteristic facies, dental anomalies, small hands and feet, and at least 2 of the following: Low-set ears Widely spaced eyes Small mandible Fifth-digit clinodactyly Syndactyly[sites.google.com]

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