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954 Possible Causes for Myopia, Possibly Scoliosis, Tall Stature

Did you mean: Myopia, Possibly, Scoliosis, Tall Stature

  • Marfan Syndrome

    Vision problems should be treated when possible. Monitor for scoliosis, especially during the teenage years.[nlm.nih.gov] The emergence of additional clinical signs (marfanoid habitus, severe myopia and dilatation of the aortic bulb) lead to consider the diagnosis of the progeroid variant of[ncbi.nlm.nih.gov] It is characterized by tall stature, elongated extremities, mitral valve prolapse, aortic dilatation, aortic dissection, and sublaxation of the lens A hereditary disorder[icd9data.com]

  • Homocystinuria

    The two diseases should be differentiated because of the thrombotic risk in homocystinuria, and also because in this disease there is a possibility of treating the biochemical[online.boneandjoint.org.uk] Further investigations disclosed lens subluxation in association with myopia, mild scoliosis and osteopenia.[ncbi.nlm.nih.gov] Autosomal recessive disease caused by cystathionine synthase deficiency Patients normal at birth, then begin to develop developmental delays History / PE : Marfan features (tall[medlibes.com]

  • Chudley-Rozdilsky Syndrome

    It may be associated with skeletal abnormalities including scoliosis, joint deformities, and hip dislocation.[linkedlifedata.com] Symptoms - Chudley Rozdilsky syndrome * Muscle disease * Curved fifth finger * Prominent ears * Small head * Short stature * Dislocated hip * Droopy eyelid * Ophthalmoplegia * Myopia[checkorphan.org] stature 60 33 hallmark (90%) Very frequent (99-80%) HP:0001519 15 downslanted palpebral fissures 60 33 hallmark (90%) Very frequent (99-80%) HP:0000494 16 hypoplasia of penis[malacards.org]

  • Stickler Syndrome

    Although common, scoliosis is generally self-limited (only one patient needed surgical treatment).[ncbi.nlm.nih.gov] In the third family, all patients had a marfanoid habitus, high myopia, and mental retardation.[ncbi.nlm.nih.gov] We describe a tall-statured 14-year-old boy who illustrated the full phenotypic and radiographic features of Stickler syndrome type I.[ncbi.nlm.nih.gov]

  • Roy-Maroteaux-Kremp Syndrome

    Syndrome dicarboxylic aminoaciduria diffuse infiltrative lymphocytosis syndrome Digitorenocerebral Syndrome Dincsoy Salih Patel Syndrome Dislocated Elbows, Bowed Tibias, Scoliosis[rgd.mcw.edu] Psychomotor Retardation, and Distinctive Facial Features cleft palate-lateral synechia syndrome Cleidorhizomelic Syndrome CLOVES syndrome COACH Syndrome Cochlear Deafness with Myopia[rgd.mcw.edu] stature-scoliosis-hearing loss syndrome CANOMAD Syndrome Cantalamessa Baldini Ambrosi Syndrome Cantu Sanchez-Corona Fragoso Syndrome Capgras syndrome capillary leak syndrome[rgd.mcw.edu]

  • Tollner-Horst-Manzke Syndrome

    Syndrome dicarboxylic aminoaciduria diffuse infiltrative lymphocytosis syndrome Digitorenocerebral Syndrome Dincsoy Salih Patel Syndrome Dislocated Elbows, Bowed Tibias, Scoliosis[rgd.mcw.edu] stature, and hearing loss syndrome Camptodactyly-ichthyosis syndrome Camptomelic syndrome long limb type Camurati Engelmann disease, type 2 Camurati-Engelmann disease Canavan[rarediseases.info.nih.gov] Psychomotor Retardation, and Distinctive Facial Features cleft palate-lateral synechia syndrome Cleidorhizomelic Syndrome CLOVES syndrome COACH Syndrome Cochlear Deafness with Myopia[rgd.mcw.edu]

  • Prader-Willi Syndrome

    The literature dealing with scoliosis surgery in PWS consists of only few case reports.[ncbi.nlm.nih.gov] Seven patients (15%) had myopia greater than -3.75 diopters. Nineteen (41%) patients had astigmatism of 1.25 diopters or greater.[ncbi.nlm.nih.gov] However, these three individuals also have features not typical of classical PWS, including tall stature as a child, large head circumference, lack of a “PWS facial gestalt[nature.com]

  • Brittle Cornea Syndrome

    In addition, the patient usually suffers from hearing loss, mental retardation, hyperextensibility of skin and joints, as well as varying degrees of scoliosis.[ncbi.nlm.nih.gov] We report a 6-week-old white boy of nonconsanguineous parents who presented with bluish scleral discoloration, thin corneas, and progressive high myopia.[ncbi.nlm.nih.gov] […] scarring of skin ; Autosomal recessive inheritance ; Blue sclerae ; Congenital hip dislocation ; Decreased corneal thickness ; Dentinogenesis imperfecta ; Disproportionate tall[mousephenotype.org]

  • Sotos Syndrome

    Other possible symptoms and signs can include: behavioral disturbances, intellectual disability, scoliosis, seizures, heart defects, kidney defects, weak muscle tone, stuttering[medicinenet.com] […] manifest the some of the following signs and symptoms: Juvenile glaucoma Poorly coordinated posture Visual deficit Juvenile onset open angle glaucoma Childhood glaucoma, myopia[syndromespedia.com] Constitutional tall stature Tall stature in childhood usually presents less initial concern than short stature because, at least in early childhood, being tall can be advantageous[childgrowthfoundation.org]

  • MASS Syndrome

    […] disorder; furthermore, due to the similarities between these two disorders, individuals with MASS syndrome follow the same treatment plans as those with Marfan syndrome.Other possible[en.wikipedia.org] […] by pectus excavatum and tall stature in the proband and tall stature in the relatives had a mutation in FBN1.[doi.org] […] with MASS syndrome follow the same treatment plans as those with Marfan syndrome. [5] Other possible symptoms are mitral valve prolapse, a large aortic root diameter, and myopia[en.wikipedia.org]

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