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70 Possible Causes for Dolichocephaly, Osteomalacia

  • Familial Hypophosphatemia

    Applicable To Vitamin D-resistant osteomalacia Vitamin D-resistant rickets Type 1 Excludes Type 1 Excludes Help A type 1 excludes note is a pure excludes.[] […] knots, similar to beads; this is called rachitic rosary Hip deformities (coxa vara) Short stature Tooth decay and abscess formation; late eruption of teeth Narrow head (dolichocephaly[] In adults, manifestations of XLH include osteomalacia, degenerative joint disease, enthesopathy, bone and joint pain, and continued dental disease.[]

  • Hypophosphatasia

    Thus, HPP features rickets or osteomalacia and hypomineralization of teeth.[] The findings in Tutankhamun include: a delicate stature the significant skull form of all family members (dolichocephaly), which is also typical for HPP partially fused neck[] A bone biopsy showed marked osteomalacia with low osteoblast numbers and greatly elevated pyrophosphate concentrations at mineralizing surfaces.[]

  • Hypophosphatemia

    Oncogenic osteomalacia is a rare clinical entity characterized by hypophosphatemia, phosphaturia, and a low concentration of 1,25-dihydroxyvitamin D(3) caused by a neoplasm[] […] knots, similar to beads; this is called rachitic rosary Hip deformities (coxa vara) Short stature Tooth decay and abscess formation; late eruption of teeth Narrow head (dolichocephaly[] This case illustrates the diagnostic difficulties in establishing a diagnosis tumor-induced osteomalacia and in identifying the responsible tumor.[]

  • X-Linked Hypophosphatemia

    Four patients with oncogenic osteomalacia had concentrations ranging from 426 to 7970 RU per milliliter, which normalized after tumor resection.[] […] knots, similar to beads; this is called rachitic rosary Hip deformities (coxa vara) Short stature Tooth decay and abscess formation; late eruption of teeth Narrow head (dolichocephaly[] All patients had moderate to severe osteomalacia at baseline as assessed by histomorphometric indices of osteomalacia.[]

  • Hypocalcemic Vitamin D-Dependent Rickets

    Clinical science Summary Bone softening caused by impaired mineralization manifests as either osteomalacia or rickets.[] […] vertebral bodies ; Abnormality of the hip bone ; Abnormality of the metaphysis ; Abnormality of the skin ; Abnormality of the thorax ; Alopecia ; Bone cyst ; Bone pain ; Dolichocephaly[] lipodystrophy - Abnormal gait - Abnormal vertebral size / shape - Alopecia - Anomalies of chest / thorax / trunk - Anomalies of skin, subcutaneous tissue and mucosae - Dolichocephaly[]

  • Platybasia

    Pathology Aetiology congenital achondroplasia Down syndrome Chiari malformations craniocleidodysostosis craniofacial anomalies osteogenesis imperfecta acquired Paget disease osteomalacia[] Limbs hip : Dislocation of hip / Hip dysplasia feet ( Club foot, Flat feet, Pes cavus ) head, face, spine and chest: skull, face and jaw ( Dolichocephaly, Plagiocephaly )[] This condition may also occur in association with bone diseases such as osteomalacia and Paget disease of bone in adulthood. In… Read More[]

  • Laron Syndrome with Immunodeficiency

    Pseudohypoparathyroidism E20.8 Other hypoparathyroidism E20.9 Hypoparathyroidism, unspecified Parathyroid tetany E21 Hyperparathyroidism and other disorders of parathyroid gland Excludes: osteomalacia[] Hypertelorism - Hypoplastic maxillary bones / zygomatic bones / maxillary hypoplasia - Macrocephaly / macrocrania / megalocephaly / megacephaly Frequent - Dental malocclusion - Dolichocephaly[] […] hair Thick lower lip vermilion Low posterior hairline Cyanosis Arnold-Chiari malformation Dandy-Walker malformation Webbed neck High, narrow palate Ichthyosis Carious teeth Dolichocephaly[]

  • Coxa Vara

    Patients who have sustained hip traumas, or suffer from osteomalacia, deforming arthritis or osteomyelitis, should be closely monitored in order to diagnose coxa vara as early[] […] hip / Hip dysplasia - Upington disease feet ( Club foot, Flat feet, Pes cavus ) systemic dislocations Larsen syndrome head, face, spine and chest : skull, face and jaw ( Dolichocephaly[] Osteomalacia. •Fibrous Dysplasia. •Infection. •Tumor. •Pagets Disease. •Pathological Fracture. •Fracture Malunion. 20.[]

  • Raine Syndrome

    In 1986, this condition was entered into Mendelian Inheritance In Man (MIM) as osteomalacia, sclerosing, with cerebral calcification (MIM 259660).[] .  Physical examination was significant for multiple congenital malformations including dolichocephaly, bulging wide fontanelles, narrow prominent forehead, gross bilateral[] Our findings suggest that certain homozygous FAM20C mutations can cause FGF23-related hypophosphatemic osteomalacia and indicate the multiple roles of FAM20C in bone.[]

  • Acroosteolysis Dominant Type

    […] philtrum - Micrognathia / retrognathia / micrognathism / retrognathism - Osteolysis / osteoclasia / bone destruction / erosions - Osteoporosis / osteopenia / demineralisation / osteomalacia[] […] pepper pot skull) chondrocalcinosis Findings in secondary (and tertiary) hyperparathyroidism are often associated with the osteosclerosis of renal osteodystrophy and the osteomalacia[] Lateral and posterior-anterior roentgenogram of skull at age 14 years: dolichocephaly and brachyeephaly; persistent nomcalcification of sutures; progressive elongation of[]

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