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330 Possible Causes for Camptodactyly (Progressive

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  • Cystitis

    Progressive coxa vara deformity and/or noninflammatory pericardial or pleural effusions are found in some patients (summary by Faivre et al., 2000).[ncbi.nlm.nih.gov] […] vara-pericarditis syndrome is an autosomal recessive condition characterized by the association of congenital or early-onset camptodactyly and noninflammatory arthropathy[ncbi.nlm.nih.gov] •Concept ID: C1855175 • Disease or Syndrome Camptodactyly arthropathy coxa vara pericarditis syndrome MedGen UID: 349226 •Concept ID: C1859690 • Disease or Syndrome The camptodactyly-arthropathy-coxa[ncbi.nlm.nih.gov]

  • Cystocele

    Progressive coxa vara deformity and/or noninflammatory pericardial or pleural effusions are found in some patients (summary by Faivre et al., 2000).[ncbi.nlm.nih.gov] […] vara-pericarditis syndrome is an autosomal recessive condition characterized by the association of congenital or early-onset camptodactyly and noninflammatory arthropathy[ncbi.nlm.nih.gov] •Concept ID: C1855175 • Disease or Syndrome Camptodactyly arthropathy coxa vara pericarditis syndrome MedGen UID: 349226 •Concept ID: C1859690 • Disease or Syndrome The camptodactyly-arthropathy-coxa[ncbi.nlm.nih.gov]

  • Coxa Vara

    Progressive coxa vara deformity and/or noninflammatory pericardial or pleural effusions are found in some patients (summary by Faivre et al., 2000).[ncbi.nlm.nih.gov] […] vara-pericarditis syndrome is an autosomal recessive condition characterized by the association of congenital or early-onset camptodactyly and noninflammatory arthropathy[ncbi.nlm.nih.gov] •Concept ID: C1855175 • Disease or Syndrome Camptodactyly arthropathy coxa vara pericarditis syndrome MedGen UID: 349226 •Concept ID: C1859690 • Disease or Syndrome The camptodactyly-arthropathy-coxa[ncbi.nlm.nih.gov]

  • Cold-Induced Sweating Syndrome Type 1

    , and progressive kyphoscoliosis (summary by {1:Hahn et al., 2010}).[diseaseinfosearch.org] Characteristic dysmorphic features include round face, chubby cheeks, micrognathia, camptodactyly, and progressive kyphoscoliosis.[cags.org.ae] In infancy and childhood they develop progressing kyphoscoliosis and developmental delay.[saudijhealthsci.org]

  • Marfan Syndrome

    ., camptodactyly), as do the toes. Hip contractures, adducted thumbs, and clubfoot may occur.[ncbi.nlm.nih.gov] Kyphosis/scoliosis, present in approximately half of all affected individuals, begins as early as infancy and is progressive.[ncbi.nlm.nih.gov]

  • Arthropathy

    OBJECTIVE: To define the molecular basis of a multisystem phenotype with progressive musculoskeletal disease of the hands and feet, including camptodactyly, subluxation, and[ncbi.nlm.nih.gov]

  • Winchester Syndrome

    […] syndrome (Common mutation) ashwindalal@gmail.com PRICKLE Progressive myoclonic epilepsy with ataxia shubharaophadke@gmail.com; sgpgigenetics@gmail.com PSAP Metachromatic[iamg.in] Sotos syndrome shubharaophadke@gmail.com; sgpgigenetics@gmail.com PEX-7 (Exons 10) Rhizomelicchondodysplasiapunctata shubharaophadke@gmail.com; sgpgigenetics@gmail.com PRG4 Camptodactyly-arthropathy-coxavara-pericarditis[iamg.in]

  • Erythroderma Desquamativum

    […] occipital calcifications Epilepsy progressive myoclonic type 2 Epilepsy telangiectasia Epilepsy with myoclono-astatic crisis Epilepsy, benign occipital Epilepsy, myoclonic progressive[bioreference.net] […] lobe type Epilepsy, partial, familial Epilepsy Epimerase deficiency Epimetaphyseal dysplasia cataract Epimetaphyseal skeletal dysplasia Epiphyseal dysplasia dysmorphism camptodactyly[bioreference.net]

  • Kohlschütter-Tönz Syndrome

    Scoliosis Cataract Macrocephaly Agenesis of corpus callosum Micropenis Abnormality of the dentition Flat occiput Postnatal microcephaly Microretrognathia Short nose Progressive[mendelian.co] […] hearing impairment Recurrent infections Retrognathia Kyphosis Clinodactyly Hypoplasia of the corpus callosum Tremor Neonatal hypotonia Intellectual disability, moderate Camptodactyly[mendelian.co]

  • Arthrogryposis Multiplex Congenita

    DA1A 108120 9p13.3 Type 1AB Camptodactyly. Talipes equinovarus. Hypoplastic finger creases.[scielo.br] COFS 214150 10q11.23 Pena-Shokeir syndrome, type II Autosomal recessive progressive neurodegenerative disorder. Microcephaly, cataracts, mental retardation.[scielo.br]

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