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20 Possible Causes for Genu Valgum, Variable Expressivity of Each Feature

  • Marfan Syndrome

    Marfan syndrome can affect many parts of the body, and each person is affected differently. This is called variable expression .[marfan.org] The prevalence is 1/20,000 and the disorder is inherited with variable expression.[encyclopedia.com] Special tests are often needed to detect these features. What does Marfan syndrome look like?[marfan.org]

  • Cenani Syndactylism

    valgum Genu varum Genu recurvatum Discoid meniscus Congenital patellar dislocation Congenital knee dislocation foot deformity: varus Club foot Pigeon toe valgus Flat feet[theinfolist.com] Although some phenotypic overlap between the various types was observed, each type had its distinguishing features.[youscribe.com] valgum Genu varum Genu recurvatum Discoid meniscus Congenital patellar dislocation Congenital knee dislocation foot deformity : varus Club foot Pigeon toe valgus Flat feet[worldebooklibrary.net]

  • Congenital Deformities of Limbs

    Genu Varum is condition when the legs bow outward; genu valgum is the condition when they bow inward (knock-knee).[ummchealth.com] EEC syndrome: Each of the three main features of ectrodactyly, ectodermal dysplasia and clefting syndrome shows a variable degree of expressivity.[oandplibrary.org] For example, in children with longitudinal fibular deficiency, the lateral femoral growth plate is often affected, causing progressive genu valgum.[now.aapmr.org]

  • Mesoaxial Synostotic Syndactyly with Phalangeal Reduction

    Ranganath P, Dalal AB .(2013) Congenital metacarpal pseudoarthrosis, cleft palate, short stature, advanced bone age, and genu valgum: a new syndrome or a variant of Devriendt[cdfd.org.in] Although some phenotypic overlap between the various types was observed, each type had its distinguishing features.[en.youscribe.com] All variants were reported to exhibit autosomal dominant inheritance with variable expression and incomplete penetrance.[en.youscribe.com]

  • Autosomal Dominant Mental Retardation Type 21

    Mental retardation, ectopia lentis, sparse blond hair, genu valgum, failure to thrive, thromboembolic episodes, fatty changes of liver.[kumc.edu] EEC syndrome: Each of the three main features of ectrodactyly, ectodermal dysplasia and clefting syndrome shows a variable degree of expressivity.[oandplibrary.org] Takenouchi-Kosaki Syndrome Tamari Goodman Syndrome TATTON-BROWN-RAHMAN SYNDROME Teebi Shaltout Syndrome Teebi Syndrome Teeth Noneruption of with Maxillary Hypoplasia and Genu[rgd.mcw.edu]

  • Autosomal Dominant Hereditary Sensory and Autonomic Neuropathy

    valgum, club foot, deformed toes; more common in males overlap syndromes see mixed connective tissue diseases patellofemoral joint syndrome see syndrome, runner's-knee peroneal[medical-dictionary.thefreedictionary.com] Each HSAN disorder is likely caused by genetic errors that affect specific aspects of small fiber neurodevelopment, which result in variable phenotypic expression. [3] HSAN[ijpd.in] Clinical features, diagnosis and treatment For each of the HSAN disorders, penetrance is complete but there can be marked variability in expression.[ojrd.biomedcentral.com]

  • Familial Dysautonomia

    valgum, club foot, deformed toes; more common in males overlap syndromes see mixed connective tissue diseases patellofemoral joint syndrome see syndrome, runner's-knee peroneal[medical-dictionary.thefreedictionary.com] Clinical features, diagnosis and treatment For each of the HSAN disorders, penetrance is complete but there can be marked variability in expression.[doi.org] […] atrophy) ( see Table 8 ) Nievergelt–Pearlman syndrome rare autosomal-dominant bone disease causing lower-limb ‘rhomboidal’ tibia/fibula (crura rhomboidei), joint dysplasias, genu[medical-dictionary.thefreedictionary.com]

  • Treft-Sanborn-Carey Syndrome

    […] primary TRAPS (TNF-receptor-associated periodic syndrome) Taurodontia absent teeth sparse hair Teebi Naguib Alawadi syndrome Teeth noneruption of with maxillary hypoplasia and genu[mindmappedia.com] When a person with ADOA plus has children, each child has a: 50% chance to have ADOA plus 50% chance not to have ADOA plus ADOA plus shows features called variable expressivity[rarediseases.info.nih.gov] T-cell lymphoma Te Tee-Ten Teebi Kaurah syndrome Teebi Naguib Alawadi syndrome Teebi Shaltout syndrome Teebi syndrome Teeth noneruption of with maxillary hypoplasia and genu[bionity.com]

  • Weyers Ulnar Ray - Oligodactyly Syndrome

    valgum Genu varum Genu recurvatum Discoid meniscus Congenital patellar dislocation Congenital knee dislocation foot deformity : varus Club foot Pigeon toe valgus Flat feet[worldebooklibrary.net] EEC syndrome: Each of the three main features of ectrodactyly, ectodermal dysplasia and clefting syndrome shows a variable degree of expressivity.[oandplibrary.org] valgum Mosaic trisomy 14 Charcot-Marie-Tooth disease Charcot-Marie-Tooth disease Dystelephalangy Microphthalmia syndromic 8 Acheiropody Short stature deafness neutrophil[checkrare.com]

  • Absence or Deformity of Leg- Cataract Syndrome

    valgum on the left side and genu varum on the right side (fig. 1).[smw.ch] EEC syndrome: Each of the three main features of ectrodactyly, ectodermal dysplasia and clefting syndrome shows a variable degree of expressivity.[oandplibrary.org] The prevalence is 1/20,000 and the disorder is inherited with variable expression.[encyclopedia.com]

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