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2 diagnostice diferențiale pentru erythrokeratodermia congenitala

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  • Nanism Hanhart

    BEARE-STEVENSON SYNDROME BEASLEY-COHEN - EHLERS-DANLOS SYNDROME WITH MENTAL RETARDATION BECKWITH-WIEDEMANN (EMG) SYNDROME BEEMER (1988) - PTOSIS; TELECANTHUS BEEMER-ROBINOW - CONGENITAL[iqb.es] DEPRESSED SCARS/PITS BEALS (1967) - AURICULO-OSTEODYSPLASIA BEARDWELL (1969) - ANKYLOSING SPONDYLITIS AND TYLOSIS BEARE (1952) - PILI TORTI; ONYCHODYSPLASIA BEARE (1972) - ERYTHROKERATODERMA[iqb.es]

  • Paraplegie spastică - ataxie - retard mental

    , WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IgE 609165 ERYTHRODERMA, ICHTHYOSIFORM, CONGENITAL RETICULAR 227090 ERYTHRODERMA, LETHAL CONGENITAL 609313 ERYTHROKERATODERMIA[wikidoc.org] TRANSPORTER DEFECT 133100 ERYTHROCYTOSIS, FAMILIAL, 1 263400 ERYTHROCYTOSIS, FAMILIAL, 2 609820 ERYTHROCYTOSIS, FAMILIAL, 3 611783 ERYTHROCYTOSIS, FAMILIAL, 4 615508 ERYTHRODERMA, CONGENITAL[wikidoc.org]

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