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448 Possible Causes for Rib Fusion

  • Polysyndactyly

    Overview Short ribs - craniosynostosis - polysyndactyly: A very rare syndrome characterized mainly by short ribs, premature fusion of skull bones and webbed fingers.[checkorphan.org] […] the 27 symptoms listed below: * Short ribs * Premature fusion of skull bones * Unusual head shape * Webbed fingers * Low set ears * Small jaw * Small mouth * Narrow ribcage[checkorphan.org] * Low set ears * Narrow ribcage * Premature fusion of skull bones * Protruding eyes * Short head * Short neck * Short ribs * Short stature * Small jaw * Small mouth * Under[checkorphan.org]

  • Anophthalmia or Microphthalmia - Esophageal Atresia Syndrome

    0001264 Spastic tetraplegia 0002510 Specific learning disability 0001328 Supernumerary ribs Extra ribs 0005815 Vertebral fusion Spinal fusion 0002948 Vertebral hypoplasia[rarediseases.info.nih.gov] […] as children 0008897 Rib fusion Fused ribs 0000902 Sensorineural hearing impairment 0000407 Short stature Decreased body height Small stature [ more ] 0004322 Spastic diplegia[rarediseases.info.nih.gov] Absent ribs Decreased rib number [ more ] 0000921 Muscular hypotonia Low or weak muscle tone 0001252 Optic nerve hypoplasia 0000609 Postnatal growth retardation Growth delay[rarediseases.info.nih.gov]

  • Renal Cysts

    In addition to the odontogenic cysts, hypertelorism, scapula deformity, rib fusion, dural calcification, and short fourth metacarpal bones of the syndrome, the patient had[ncbi.nlm.nih.gov]

  • Mitochondrial Myopathy

    Multiple anomalies were also identified, including rib fusions, ventricular septal dyskinesis, and mild hypotonia. Initial chromosome studies were unremarkable.[ncbi.nlm.nih.gov]

  • Monosomy 1p36 Syndrome

    fusion Fused ribs 0000902 Scoliosis Abnormal curving of the spine 0002650 Sensorineural hearing impairment 0000407 Short stature Decreased body height Small stature [ more[rarediseases.info.nih.gov] […] pigmentation in the eye 0001107 Optic atrophy 0000648 Patent ductus arteriosus 0001643 Polyphagia Voracious appetite 0002591 Pyloric stenosis 0002021 Renal cyst Kidney cyst 0000107 Rib[rarediseases.info.nih.gov]

  • Autosomal-Recessive Robinow Syndrome

    fusions, which is not seen in the dominant form.[ncbi.nlm.nih.gov] fusion, brachydactyly (shortening of the digits), congenital heart disease, genital hypoplasia, and dysmorphic facial features with gum hypertrophy.[link.springer.com] Rib fusions are considered to be characteristic of the autosomal recessive form.[uniprot.org]

  • Dysostosis

    The main feature include dwarfism, vertebral fusion, hemivertebrae, posterior rib fusion, reduced rib number, and other rib malformations.[uniprot.org] The main skeletal malformations include fusion of the vertebrae, hemivertebrae, and rib fusion with other rib malformations.[orpha.net] . 0001511 Respiratory insufficiency Respiratory impairment 0002093 Rib fusion Fused ribs 0000902 Rib segmentation abnormalities 0006655 Scoliosis Abnormal curving of the spine[rarediseases.info.nih.gov]

  • Becker Nevus Syndrome

    fusion Fused ribs 0000902 Scoliosis Abnormal curving of the spine 0002650 Spina bifida occulta 0003298 Supernumerary ribs Extra ribs 0005815 Upper limb asymmetry 0100560[rarediseases.info.nih.gov] […] of the shinbone [ more ] 0002992 Hypoplastic labia minora Underdeveloped inner lips 0000064 Kyphosis Hunched back Round back [ more ] 0002808 Lower limb asymmetry 0100559 Rib[rarediseases.info.nih.gov]

  • Urioste Martinez-Frias Syndrome

    Observe bone bridging resulting in rib fusion (fifth and sixth ribs) and pseudarthrosis (seventh and eighth).Also note multiple rib fusion on both sides and hypoplastic/absent[rrnursingschool.biz] Forked ribs are more common than rib fusion (Guttentag and Salwen 1999). Bifurcation consists in duplication of the anterior portion of the rib, most often the fourth.[rrnursingschool.biz] Defects in Segmentation [Fusion or bifurcation of the ribs] Segmentation defects are the third most common (20 %) congenital anomalies affecting the ribs, after supernumerary[rrnursingschool.biz]

  • Robinow Syndrome

    Using the presence of rib fusions as diagnostic of the recessive variant, and also based on the inheritance pattern in familial cases, we classified 37 patients as having[ncbi.nlm.nih.gov] fusions, which is not seen in the dominant form.[ncbi.nlm.nih.gov] Rib fusions appear to be present almost exclusively in the autosomal recessive form.[orpha.net]

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