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7 Possible Causes for Juvenile Familial Leg Ulcers

  • 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]

  • 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]

  • Waters-West Syndrome

    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] […] of, with Congenital Cataract OMIM:150600 Legg-Calve-Perthes Disease; LCPD OMIM:608556 Legionnaire Disease, Susceptibility to OMIM:611431 Legius Syndrome; LGSS OMIM:150590 Leg[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]

  • Lethal Congenital Contracture Syndrome 6

    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] […] of, with Congenital Cataract OMIM:150600 Legg-Calve-Perthes Disease; LCPD OMIM:608556 Legionnaire Disease, Susceptibility to OMIM:611431 Legius Syndrome; LGSS OMIM:150590 Leg[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]

  • 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]

  • Leukoencephalopathy - Metaphyseal Chondrodysplasia Syndrome

    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] […] of, with Congenital Cataract OMIM:150600 Legg-Calve-Perthes Disease; LCPD OMIM:608556 Legionnaire Disease, Susceptibility to OMIM:611431 Legius Syndrome; LGSS OMIM:150590 Leg[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]

  • Progeroid Syndrome Type Petty

    ulcers juvenile cataracts hypogonadism, which is associated with reduced fertility tendency to develop diabetes calcification of blood vessels osteoporosis metastatic calcification[plasticsurgerykey.com] […] tendency to occur in families.[plasticsurgerykey.com] […] is in the second decade premature greying of the hair, with age of onset in the early 20s premature baldness, with onset in the 20s scleropoikiloderma-like skin trophic leg[plasticsurgerykey.com]

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