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1,207 Possible Causes for TD 60

Did you mean: TD, 60

  • Pharyngitis

    Kocher, JJ; Selby, TD (1 July 2014). "Antibiotics for sore throat.". American family physician . 90 (1): 23–4. PMID 25077497 .[ipfs.io] European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology . 32 (2): 151–60. PMID 22993127 .[ipfs.io]

  • Osteoporosis

    Outwardly difficult to distinguish, OI type II, thanatophoric dysplasia , campomelic dysplasia, and chondrodysplasias with bone mineralization defects are readily distinguished[ncbi.nlm.nih.gov]

  • Thanatophoric Dysplasia

    […] the thanatophoric dysplasia fetuses from the others with skeletal dysplasias like fibrochondrogenesis or atelosteogenesis by ultrasonography.[ncbi.nlm.nih.gov] Thanatophoric Dysplasia, Type I[ncbi.nlm.nih.gov] Abstract Bony abnormalities caused by thanatophoric dysplasia affect the base of the skull and the vertebrae as well as the ribs and appendicular long bones.[ncbi.nlm.nih.gov]

  • Thanatophoric Dysplasia 2

    Thanatophoric dysplasia 2 is an autosomal dominant disorder caused by mutations of the FGFR3 gene. It is characterized by a short-limb dwarfism.[moldiag.com] Alternate Names Type 2 Thanatophoric Dysplasia is also known as Thanatophoric Dysplasia, Type 2, Thanatophoric Dysplasia, Type Ii.[novusbio.com] Prognosis - Thanatophoric dysplasia- type 2 Not supplied. Treatment - Thanatophoric dysplasia- type 2 Not supplied.[checkorphan.org]

  • Thanatophoric Dysplasia Type 1

    According to the literature, cloverleaf skull in thanatophoric dysplasia type 1 is rare, even more so in dichorionic twins.[ncbi.nlm.nih.gov] Thanatophoric dysplasia is a type of short-limbed neonatal dwarfism that is usually lethal in the perinatal period.[ncbi.nlm.nih.gov] Thanatophoric dysplasia. Indian Pediatr 1994;31:1405-10. Tirumalasetti N. Case report of thanatophoric dysplasia: A lethal skeletal dysplasia.[axisjournals.com]

  • Thanatophoric Dysplasia Glasgow Variant

    […] be the full list of Thanatophoric dysplasia, Glasgow variant signs or Thanatophoric dysplasia, Glasgow variant symptoms.[checkorphan.org] Western Abstracts: Morphogenesis and Malformations Concurrent Session 1:30 PM: Friday, February 3, 2006 333 GLASGOW VARIANT OF THANATOPHORIC DYSPLASIA: EXPANDING THE PHENOTYPE[jim.bmj.com] Prognosis - Thanatophoric dysplasia Glasgow variant Not supplied. Treatment - Thanatophoric dysplasia Glasgow variant Not supplied.[checkorphan.org]

  • Skeletal Dysplasia

    Dysplasia/diagnosis* Thanatophoric Dysplasia/genetics* Substances Codon Receptor, Fibroblast Growth Factor, Type 3 Supplementary concept Thanatophoric Dysplasia, Type I[ncbi.nlm.nih.gov] They display a spectrum of severity in the skeletal findings, ranging from relatively mild hypochondroplasia to lethal thanatophoric dysplasia.[ncbi.nlm.nih.gov] dysplasia.[ncbi.nlm.nih.gov]

  • Achondroplasia

    Thanatophoric dysplasia, hypochondroplasia and achondroplasia are all caused by FGFR3 (fibroblast growth factor receptor 3) mutations.[ncbi.nlm.nih.gov] Achondroplasia, hypochondroplasia, and thanatophoric dysplasia are syndromes of short-limbed dwarfism caused by activating mutations of fibroblast growth factor receptor-3[ncbi.nlm.nih.gov] We report two patients with clinical and radiological findings of achondroplasia, who had the most common FGFR3 mutation occurring in thanatophoric dysplasia type I and hypochondroplasia[ncbi.nlm.nih.gov]

  • Platyspondyly

    DISORDERS THAT HAVE PLATYSPONDYLY Thanatophoric dysplasia. Osteogenesis imperfecta Type II. Morquio's syndrome.[fetalultrasound.com] From Etiology osteogenesis imperfecta type2 ( congenital platyspondyly). thanatophoric dysplasia metatropic dwarfism Morquios disease (develops later childhood) spondyloepiphyseal[anvita.info] -multiple flattened vertebral bodies -if there's only one flattened vertebral body vertebra plana -congenital platyspondyly thanatophoric dysplasia metatropic dwarfism OI[raded.wikidot.com]

  • Hypochondroplasia

    BACKGROUND: Thanatophoric dysplasia (TD) and hypochondroplasia are both caused by FGFR3 (fibroblast growth factor receptor 3) gene mutations.[ncbi.nlm.nih.gov] We suggest FGFR3 mutations might cause cerebral malformations in hypochondroplasia as well as in thanatophoric dysplasia.[ncbi.nlm.nih.gov] Specific mutations in the FGFR3 gene are associated with autosomal dominant human skeletal disorders such as hypochondroplasia, achondroplasia, and thanatophoric dysplasia[ncbi.nlm.nih.gov]

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