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329 Possible Causes for Poikiloderma, Small Foot

  • Rothmund Thomson Syndrome

    This report confirms the clinical and genetic identity of the Clericuzio type of poikiloderma with neutropenia syndrome.[ncbi.nlm.nih.gov] […] eyeball 0000568 Osteoporosis 0000939 Short foot Short feet Small feet [ more ] 0001773 Short nose Decreased length of nose Shortened nose [ more ] 0003196 Short palm 0004279[rarediseases.info.nih.gov] Two sisters with congenital poikiloderma (Rothmund-Thomson syndrome) are described.[ncbi.nlm.nih.gov]

  • Autosomal Recessive Spastic Paraplegia Type 20

    Spastic paraplegia neuropathy poikiloderma 0 *Rothmund-Thomson Syndrome *Spastic Paraplegia, Hereditary.[reference.md] When present it is found in distal muscles in the lower limbs, usually the small muscles of the foot and tibialis anterior.[jnnp.bmj.com]

  • Acrootoocular Syndrome

    Cornea RDC 180550 Genetic Test Registry Roberts Syndrome Long Bone Deficiencies Associated With Cleft Lip-Palate RBS 268300 Genetic Test Registry Rothmund-Thomson Syndrome Poikiloderma[ukgtn.nhs.uk]

  • RAPADILINO Syndrome

    Mutations of the RECQL4 gene have also been described for these syndromes.The presence of poikiloderma, a major symptom of RTS, distinguishes this syndrome from RAPADILINO[orpha.net] Constipation and irritable bowel syndrome are more common Flat foot or pes planus is seen in the majority of patients with the nail-patella syndrome.[boneandspine.com] While many features of the 2 genetic disorders overlap, poikiloderma—a hallmark of RTS—has been described as generally absent in RAPADILINO syndrome.[jamanetwork.com]

  • Parapsoriasis

    Both types of poikiloderma were similar with regard to T-cell antigen expression.[ncbi.nlm.nih.gov] We describe a 55-year-old female with a pruritic erythematous nodule on the lateral aspect of her right foot present for 1.5 years.[thedoctorsdoctor.com] Abstract Thirty-five cases of benign parapsoriasis en plaques, 24 cases of prereticulotic poikiloderma (3 of which were in evolution towards polymorphous lymphomas), 15 cases[ncbi.nlm.nih.gov]

  • Prata-Libéral-Gonçalves Syndrome

    […] congenital with bullae Weary type Poikiloderma hereditary acrokeratotic Weary type Poikiloderma of Rothmund-Thomson Poikilodermatomyositis mental retardation Poikilodermia[mindmappedia.com] […] delay Caudal appendage Aplastic clavicle Carpal bone hypoplasia Abnormality of the rib cage Abnormality of the face Abnormality of epiphysis morphology Abnormality of the foot[mendelian.co] […] congenital with bullae Weary type Poikiloderma hereditary acrokeratotic Weary type Poikiloderma of Kindler Poikiloderma of Rothmund-Thomson Poikilodermatomyositis mental[bioreference.net]

  • Oculocerebral Hypopigmentation Syndrome Type Cross

    ( Poikiloderma of Civatte · Poikiloderma vasculare atrophicans ) · Riehl melanosis Linear Incontinentia pigmenti · Scratch dermatitis · Shiitake mushroom dermatitis Other[wiki30.com] […] hand Short foot Nail dystrophy Skin erosion Aplasia/Hypoplasia of the patella Tetralogy of Fallot Telecanthus Broad nasal tip Single transverse palmar crease Everted lower[mendelian.co] ( Poikiloderma of Civatte Poikiloderma vasculare atrophicans ) Riehl melanosis Linear Incontinentia pigmenti Scratch dermatitis Shiitake mushroom dermatitis Other/ ungrouped[en.wikipedia.org]

  • Mycosis Fungoides

    Poikiloderma occurs in many different clinical conditions, which makes a diagnostic procedure more complicated.[ncbi.nlm.nih.gov] Primary cutaneous CD4 small/medium T-cell lymphoproliferative disorder often starts as a single area of thickening of the skin or a tumor on the head, neck, or upper body.[cancer.org] Poikiloderma atrophicans vasculare. Arch Dermatol 1971;103:550 [ PubMed ] 5. Kreuter A, et al.[escholarship.org]

  • Tendinitis

    Mitochondria Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy Orbital Myositis Pectoralis Muscle, Absence of Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss Poikiloderma[rgd.mcw.edu] The end of the shinbone of the leg (tibia) and a small bone in the leg (fibula) meet a large bone in the foot, called the talus, to form the ankle.[medicinenet.com] Speeding up For now, use slow speeds of movement, relatively small ranges of motion, and low resistance (just your body weight) for exercises three through five.[sportsinjurybulletin.com]

  • Pfeiffer-Palm-Teller Syndrome

    […] congenital with bullae Weary type Poikiloderma hereditary acrokeratotic Weary type Poikiloderma of Kindler Poikiloderma of Rothmund-Thomson Poikilodermatomyositis mental[bioreference.net] […] hand Infertility Short foot Downturned corners of mouth Polymicrogyria Short palm Short philtrum Delayed puberty Pruritus Neonatal hypotonia Photophobia Upslanted palpebral[mendelian.co] Poikiloderma congenital with bullae Weary type[?] Poikiloderma hereditary acrokeratotic Weary type[?] Poikiloderma of Kindler[?] Poikiloderma of Rothmund-Thomson[?][encyclopedia.kids.net.au]

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