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150 Possible Causes for Kyphoscoliosis, Postural Defect

  • Homocystinuria

    […] appearance reminiscent of Marfan syndrome ) Pectus carinatum or pectus excavatum (the depression of protrusion of the sternum) High, arched palate with crowding of the teeth Kyphoscoliosis[dermnetnz.org] […] failure to thrive in infancy), fine, brittle hair, hypopigmentation, high arched palate, crowded teeth, arachnodactyly, limited joint mobility, pectus excavatum/carinatum, kyphoscoliosis[patient.info] Other prominent symptoms include fine and brittle hair, decreased pigmentation of the skin, crowding of the teeth, decreased joint mobility, kyphoscoliosis, a high arched[symptoma.com]

  • Craniodiaphyseal Dysplasia

    In some cases, a postural defect in the metaphyses may also be noted.[primehealthchannel.com] The jaw was prominent and there was kyphoscoliosis of dorsal spine. The fundus examination was normal.[ijo.in] defect in the metaphyses Some of the complications of CDD are severe facial deformity, facial diplegia, complete hearing inability, nasolacrimal obstruction, quadriparesis[ehealthhall.com]

  • Cockayne Syndrome

    It consists of: Treatment of specific signs and symptoms: Physiotherapy to loosen joints, correct posture defects, and keep muscles supple Medication to relax spastic muscles[news-medical.net] CAMFAK syndrome is an inherited disease characterized by congenital cataracts, microcephaly, failure to thrive, and kyphoscoliosis with onset in early infancy.[ncbi.nlm.nih.gov] Many patients exhibit a characteristic stooped appearance with kyphoscoliosis and flexion deformities of hips, knees, and ankles.[ijpd.in]

  • Spinal Osteochondrosis

    Children suffering from postural defects, structural scoliosis and spinal osteochondrosis were separated from a normal group.[ncbi.nlm.nih.gov] Lumbosacral region 8 Sacral and sacrococcygeal region 9 Site unspecified Deforming dorsopathies (M40-M43) M40 Kyphosis and lordosis [See site code before M40] Excludes: kyphoscoliosis[apps.who.int] Key words Spinal mobility Structural scoliosis Spinal osteochondrosis Postural defects This is a preview of subscription content, log in to check access.[link.springer.com]

  • Ataxia Telangiectasia

    Defects in speech Spider-like veins visible along the skin and eyes Recurrent lung, sinus, and ear infection Slow physical and sexual maturation How is Ataxia Telangiectasia[dovemed.com] None of them presented deformities of the feet or kyphoscoliosis.[onlinelibrary.wiley.com] Eye movement abnormalities (80% of patients) with characteristic oculomotor apraxia, with nystagmus and various defects in saccade and gaze control (usually, abnormalities[raredisorders.imedpub.com]

  • PIBIDS Syndrome

    It consists of: Treatment of specific signs and symptoms: Physiotherapy to loosen joints, correct posture defects, and keep muscles supple Medication to relax spastic muscles[news-medical.net] Striae distensae, abdominal wall hernias, elastosis perforans serpiginosa, upward ectopia lentis, tall stature, hyperextensible joints, pectus excavatum, arachnodactyly, kyphoscoliosis[superteachertools.us]

  • Cerebro-Oculo-Facio-Skeletal Syndrome 1

    It consists of: Treatment of specific signs and symptoms: Physiotherapy to loosen joints, correct posture defects, and keep muscles supple Medication to relax spastic muscles[news-medical.net] […] comprised of microcephaly, hypotonia, failure to thrive, arthrogryposis, eye defects, prominent nose, large ears, overhanging upper lip, micrognathia, widely set nipples, kyphoscoliosis[datapunk.net] […] microgyria,Agenesis of corpus callosum,Infantile spasm,Hypotonia,Cerebellar hypoplasia,Subcortical gliosis,Third ventricle subependymal focal gliosis SKELETAL Osteoporosis,Spine Kyphoscoliosis[datapunk.net]

  • Cutis Laxa

    Dystonic posturing was discriminatory for PYCR1 and ALDH18A1 defects. Metabolic markers of mitochondrial dysfunction were found in one patient with PYCR1 mutations.[ncbi.nlm.nih.gov] The patient has gynecomastia, acromegaly, and kyphoscoliosis. The patient remains well at 19 months after treatment.[ncbi.nlm.nih.gov] Epilepsy was most common in ATP6V0A2 defects. Corpus callosum dysgenesis was associated with PYCR1 and ALDH18A1 mutations.[ncbi.nlm.nih.gov]

  • Cerebro-Oculo-Facio-Skeletal Syndrome

    It consists of: Treatment of specific signs and symptoms: Physiotherapy to loosen joints, correct posture defects, and keep muscles supple Medication to relax spastic muscles[news-medical.net] […] comprised of microcephaly, hypotonia, failure to thrive, arthrogryposis, eye defects, prominent nose, large ears, overhanging upper lip, micrognathia, widely set nipples, kyphoscoliosis[datapunk.net] […] distinguishing characteristics are: wrinkled ears or crushed, flexion contractures of the fingers, which are long arachnodactyly), contractures of the elbows, knees and hips, kyphoscoliosis[milyyjess.blogspot.com]

  • Cerebrooculofacioskeletal Syndrome Type 4

    It consists of: Treatment of specific signs and symptoms: Physiotherapy to loosen joints, correct posture defects, and keep muscles supple Medication to relax spastic muscles[news-medical.net] […] comprised of microcephaly, hypotonia, failure to thrive, arthrogryposis, eye defects, prominent nose, large ears, overhanging upper lip, micrognathia, widely set nipples, kyphoscoliosis[datapunk.net] […] microgyria,Agenesis of corpus callosum,Infantile spasm,Hypotonia,Cerebellar hypoplasia,Subcortical gliosis,Third ventricle subependymal focal gliosis SKELETAL Osteoporosis,Spine Kyphoscoliosis[datapunk.net]

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