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370 Possible Causes for Severe Camptodactyly

  • Freeman-Sheldon Syndrome

    Affected individuals have vertical talus, ulnar deviation, severe camptodactyly, and a distinctive face characterized by a triangular shape, prominent nasolabial folds, downslanting[ncbi.nlm.nih.gov] camptodactyly ulnar deviation equinovarus congenital kyphoscoliosis club feet Genetics It is thought to carry an autosomal dominant inheritance in most cases with occasional[radiopaedia.org] […] hypotelorism 8 : drooping of the upper eyelids : strabismus : low-set ears gradual hearing loss microcephaly musculoskeletal: arthrogryposis : joint contractures often tends to be severe[radiopaedia.org]

  • Cystitis

    OI type VII is an autosomal recessive form of severe or lethal OI (summary by Barnes et al., 2006).[ncbi.nlm.nih.gov] Metaphyseal dysostosis mental retardation conductive deafness MedGen UID: 344437 •Concept ID: C1855175 • Disease or Syndrome Camptodactyly arthropathy coxa vara pericarditis[ncbi.nlm.nih.gov]

  • Cystocele

    […] secondary to other underlying bone diseases such as: osteogenesis imperfecta cretinism dyschondroplasia(s) Paget's disease osteoporosis capital coxa vara: occasionally seen in severe[radiopaedia.org] OI type VII is an autosomal recessive form of severe or lethal OI (summary by Barnes et al., 2006).[ncbi.nlm.nih.gov] […] osteoarthritis and Legg-Perthes' disease Associations congenital dislocation of hip - developmental hip dysplasia faulty development of the femur craniocleidodysostosis camptodactyly[radiopaedia.org]

  • Chronic Fatigue Syndrome

    […] secondary to other underlying bone diseases such as: osteogenesis imperfecta cretinism dyschondroplasia (s) Paget's disease osteoporosis capital coxa vara: occasionally seen in severe[radiopaedia.org] […] osteoarthritis and Legg-Perthes' disease Associations congenital dislocation of hip - developmental hip dysplasia faulty development of the femur craniocleidodysostosis camptodactyly[radiopaedia.org]

  • Coxa Vara

    […] syndrome with the possible expansion of the phenotype to include congenital cataract. ( 22678705 ) Akawi NA...Al-Gazali L 2012 31 Total hip arthroplasty in adolescents with severe[malacards.org] […] secondary to other underlying bone diseases such as: osteogenesis imperfecta cretinism dyschondroplasia(s) Paget's disease osteoporosis capital coxa vara: occasionally seen in severe[radiopaedia.org] […] secondary to other underlying bone diseases such as: osteogenesis imperfecta cretinism dyschondroplasia (s) Paget's disease osteoporosis capital coxa vara: occasionally seen in severe[radiopaedia.org]

  • Distal Arthrogryposis Type 5D

    camptodactyly of\nthe hands, including adducted thumbs and wrists; mild camptodactyly of\nthe toes; clubfoot and/or a calcaneovalgus deformity; extension\ncontractures of[lifemodules.org] DA5D is characterized by severe camptodactyly of the hands, mild camptodactyly of the toes, clubfoot and/or a calcaneovalgus deformity, extension contractures of the knee,[ghr.nlm.nih.gov] DISTAL, TYPE 5D; DA5D OMIM ID: 615065 Description: 'This autosomal recessive form of distal arthrogryposis, designated DA5D\nby McMillin et al. (2013), is characterized by severe[lifemodules.org]

  • Psychomotor Retardation

    Prader-willi habitus associated with osteopenia and camptodactyly is known as the urban-rogers-meyer syndrome.[icd10data.com] A syndrome characterized by growth retardation, severe mental retardation, short stature, a low-pitched growling cry, brachycephaly, low-set ears, webbed neck, carp mouth,[icd10data.com]

  • Reversible Cerebral Vasoconstriction Syndrome

    The patient was a 9-year-old boy with a heterozygous TGFBR2 mutation, manifesting camptodactyly, talipes equinovarus, and lamboid craniosynostosis.[ncbi.nlm.nih.gov] He complained of severe recurrent headaches 2 months after total aortic replacement for aortic root dilatation and a massive Stanford type B aortic dissection.[ncbi.nlm.nih.gov]

  • Autosomal-Recessive Non-Lethal Multiple Pterygium Syndrome

    The hands had hypoplastic dermal ridges and palmar creases with severe camptodactyly and absent thumb abduction and extension (due to congenital webbing and contracture of[cags.org.ae] […] of the hands with hypoplastic flexion creases, vertebral fusions, severe scoliosis and short stature.[orpha.net] , camptodactyly and surgical scars on both feet.[cags.org.ae]

  • Neurogenic Arthrogryposis Multiplex Congenita

    Gordon syndrome is characterized by the permanent fixation of several fingers in a flexed position (camptodactyly), abnormal bending inward of the foot (clubfoot or talipes[web.archive.org] Type i involves primarily the distal parts of the hands and feet and is characterized by overlapping fingers, clenched fists, ulnar deviation of the fingers, camptodactyly[icd9data.com] […] micrognathia Treatment and prognosis The prognosis is highly variable and is dependent on associated anomalies and severity.[radiopaedia.org]

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