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247 Possible Causes for Caudal Dysplasia Syndrome

  • Diabetes Mellitus Type 1

    Diabetes mellitus type 1 is a class of diabetes that develops secondary to the autoimmune destruction of the pancreatic beta cells, resulting in an insulin deficiency. In patients with a clinical picture suggestive of diabetes, the evaluation consists of a thorough personal and family history including a detailed[…][symptoma.com]

  • Photosensitivity Disorder

    As a traumatic brain injury attorney, I am always interested in new information on head injury. I am proud to live in San Francisco where we can boast that our main city and county hospital has received a prestigious brain trauma certification in the treatment for traumatic brain injury (TBI). As a San Francisco[…][ccwlawyers.com]

  • Femoral Hypoplasia

    The Caudal Dysplasia syndrome and the Femoral Hypoplasia-Unusual Facies syndrome have been reported to be more frequent among infants of diabetic mothers.[ncbi.nlm.nih.gov] The Caudal dysplasia syndrome (CDS) and the femoral hypoplasia-unusual facies syndrome (FHUFS) have been reported to be more frequent among infants of diabetic mothers (IDMs[ncbi.nlm.nih.gov] The pathogenesis and natural history of FH/UFS is discussed and contrasted with the caudal dysplasia syndrome.[ncbi.nlm.nih.gov]

  • Lynch Syndrome

    […] or caudal dysplasia syndrome.[jmg.bmj.com] This should provide a basis for understanding its involvement in Currarino syndrome.[jmg.bmj.com] Differential diagnosis Isolated sacral agenesis can occur as a consequence of diabetic embryopathy or because of unknown causes where it is described as the caudal regression[jmg.bmj.com]

  • Foot Deformity

    caudal regression syndrome diastematomyelia spina bifida skeletal dysplasias diastrophic dysplasia Plain radiograph Assessment requires weight bearing DP and lateral radiographs[radiopaedia.org] Meckel Gruber syndrome Roberts syndrome renal anomalies prune belly syndrome renal agenesis connective tissue disorders Marfan syndrome Ehlers-Danlos syndrome spinal anomalies[radiopaedia.org] […] estimated at 200) 8 of associations which include: chromosomal anomalies 18q deletion syndrome trisomy 18 Wolf-Hirschhorn syndrome other syndromic conditions Freeman Sheldon syndrome[radiopaedia.org]

  • Hematocolpos

    159 513 Osteogenesis Imperfecta 161 514 Caudal Regression Syndrome and Sirenomelia Mermaid Syndrome 163 515 Ellisvan Creveld Syndrome Chondroectodermal Dysplasia 165 516[books.google.com] 149 59 Paget Disease Ostitis Deformans 151 510 Osteopetrosis AlbersSchönburg DiseaseMarble Bone Disease 153 511 Mucopolysaccharidosis 156 512 Ollier Disease and Maffucci Syndrome[books.google.com]

  • Hereditary Hyperekplexia

    Brachydactyly syndrome type C Cardio-acral-facial syndrome Cardio-facio-cutaneous syndrome Carpenter's syndrome Caudal dysplasia sequence Celosomial monster Cerebro-costo-mandibular[icd9data.com] syndrome Cerebrofacial dysplasia Cerebro-oculo-facio-skeletal syndrome Charge association Charge syndrome Child syndrome Chimera Chronic infantile neurological, cutaneous[icd9data.com] […] syndrome Biemond's syndrome Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goiter, and primary gonadal insufficiency Borjeson-Forssman-Lehmann syndrome[icd9data.com]

  • Acquired Nasolacrimal Duct Stenosis

    Dorsal Spinal Meningocele Neurofibromatosis Type 1, Spine Neurofibromatosis Type 2, Spine Dural Dysplasia Leukemia, Spine Neuroblastic Tumor Prin A.[euro-libris.ro] Regression Syndrome Tethered Spinal Cord Nonterminal Myelocystocele Terminal Myelocystocele Anterior Sacral Meningocele I Diastematomyelia Neurenteric Cyst Lateral Meningocele[euro-libris.ro] Cellular Ependymoma SECTION VI: MULTIPLE REGIONS, SPINE Myelomeningocele Lipomyelomeningocele Dorsal Dermal Sinus Dermoid Cyst Epidermoid Cyst Segmental Spinal Dysgenesis Caudal[euro-libris.ro]

  • Congenital Clubfoot

    caudal regression syndrome diastematomyelia spina bifida skeletal dysplasias diastrophic dysplasia Plain radiograph Assessment requires weight bearing DP and lateral radiographs[radiopaedia.org] Meckel Gruber syndrome Roberts syndrome renal anomalies prune belly syndrome renal agenesis connective tissue disorders Marfan syndrome Ehlers-Danlos syndrome spinal anomalies[radiopaedia.org] […] estimated at 200) 8 of associations which include: chromosomal anomalies 18q deletion syndrome trisomy 18 Wolf-Hirschhorn syndrome other syndromic conditions Freeman Sheldon syndrome[radiopaedia.org]

  • Uhl Anomaly

    159 513 Osteogenesis Imperfecta 161 514 Caudal Regression Syndrome and Sirenomelia Mermaid Syndrome 163 515 Ellisvan Creveld Syndrome Chondroectodermal Dysplasia 165 516[books.google.com] 149 59 Paget Disease Ostitis Deformans 151 510 Osteopetrosis AlbersSchönburg DiseaseMarble Bone Disease 153 511 Mucopolysaccharidosis 156 512 Ollier Disease and Maffucci Syndrome[books.google.com]

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