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21 Possible Causes for Generalized Thinning of Tubular Bones, Juvenile Familial Leg Ulcers

  • Lethal Congenital Contracture Syndrome 1

    Ulcers, Familial, of Juvenile Onset OMIM:220111 Leigh Syndrome, French Canadian Type; LSFC OMIM:256000 Leigh Syndrome; LS OMIM:150700 Leiomyoma of Vulva and Esophagus OMIM[informatics.jax.org] LVNC1 OMIM:609470 Left Ventricular Noncompaction 2; LVNC2 OMIM:615092 Left Ventricular Noncompaction 7; LVNC7 OMIM:615373 Left Ventricular Noncompaction 8; LVNC8 OMIM:246000 Leg[informatics.jax.org] Deformity of, with Congenital Cataract OMIM:150600 Legg-Calve-Perthes Disease; LCPD OMIM:608556 Legionnaire Disease, Susceptibility to OMIM:611431 Legius Syndrome OMIM:150590 Leg[informatics.jax.org]

  • Familial Normophosphatemic Tumoral Calcinosis

    Actinic Keratosis Palmaris Et Plantaris With Clinodactyly Keratosis Palmoplantaris Papulosa Kyrle Disease Lateral Meningocele Syndrome Leg Ulcers , Familial, Of Juvenile[familydiagnosis.com] Deafness Hypocalcemic Vitamin D-Resistant Rickets Hypoplasminogenemia Ichthyosis With Hypotrichosis , Autosomal Recessive Insect Stings , Hypersensitivity To Keratosis , Familial[familydiagnosis.com]

    Missing: Generalized Thinning of Tubular Bones
  • Osteogenesis Imperfecta Type 2

    Milder forms of this condition result in thin, overtubulated (gracile) bones with thin cortices and relatively few fractures (see the images below).[emedicine.medscape.com] The short tubular bones are also affected, though they are less frequently fractured.[emedicine.medscape.com] General radiographic features of osteogenesis imperfecta The radiologic sine qua non of osteogenesis imperfecta is generalized osteoporosis of both the axial and appendicular[emedicine.medscape.com]

    Missing: Juvenile Familial Leg Ulcers
  • Osteogenesis Imperfecta Type 15

    Radiologically, in OI type I, bone fragility in combination with generalized demineralization, slender shafts of tubular bones with thin cortex and poorly trabeculated spongiosa[nature.com]

    Missing: Juvenile Familial Leg Ulcers
  • Osteogenesis Imperfecta Type 3

    Milder forms of this condition result in thin, overtubulated (gracile) bones with thin cortices and relatively few fractures (see the images below).[emedicine.medscape.com] The short tubular bones are also affected, though they are less frequently fractured.[emedicine.medscape.com] General radiographic features of osteogenesis imperfecta The radiologic sine qua non of osteogenesis imperfecta is generalized osteoporosis of both the axial and appendicular[emedicine.medscape.com]

    Missing: Juvenile Familial Leg Ulcers
  • Osteogenesis Imperfecta Type 13

    Milder forms of this condition result in thin, overtubulated (gracile) bones with thin cortices and relatively few fractures (see the images below).[emedicine.medscape.com] The short tubular bones are also affected, though they are less frequently fractured.[emedicine.medscape.com] General radiographic features of osteogenesis imperfecta The radiologic sine qua non of osteogenesis imperfecta is generalized osteoporosis of both the axial and appendicular[emedicine.medscape.com]

    Missing: Juvenile Familial Leg Ulcers
  • Osteogenesis Imperfecta Type 16

    Milder forms of this condition result in thin, overtubulated (gracile) bones with thin cortices and relatively few fractures (see the images below).[emedicine.medscape.com] The short tubular bones are also affected, though they are less frequently fractured.[emedicine.medscape.com] General radiographic features of osteogenesis imperfecta The radiologic sine qua non of osteogenesis imperfecta is generalized osteoporosis of both the axial and appendicular[emedicine.medscape.com]

    Missing: Juvenile Familial Leg Ulcers
  • Schwartz-Lelek Syndrome

    Long bones are undermodeled, and bony cortices are generally thin. Tubular leg bones have gross Erlenmeyer flask flaring, particularly in the distal femur.[merckmanuals.com]

    Missing: Juvenile Familial Leg Ulcers
  • Werner Syndrome

    Neuropathy or familial leg ulcers of juvenile onset.[ncbi.nlm.nih.gov] Distal atrophy and skin ulcerations in the absence of other manifestations characteristic of Werner syndrome could raise the possibility of Charcot-Marie-Tooth Hereditary[ncbi.nlm.nih.gov]

    Missing: Generalized Thinning of Tubular Bones
  • Frontometaphyseal Dysplasia

    Long bones are undermodeled, and bony cortices are generally thin. Tubular leg bones have gross Erlenmeyer flask flaring, particularly in the distal femur.[merckmanuals.com]

    Missing: Juvenile Familial Leg Ulcers

Further symptoms