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422 Possible Causes for Ectopia Lentis, Long, Thin Fingers

  • Marfan Syndrome

    The main clinical manifestations include long limbs, long slender fingers, lens subluxation, abnormal cardiac valves, and aortic aneurysm.[] fingers and long arms and legs They may have a dislocation of the lens in the eye that also causes nearsightedness or myopia that can progress quickly They may have a detached[] We present a case of Marfan syndrome with lens coloboma in one eye and ectopia lentis in the other. A 14-year-old girl reported decreased vision in the left eye.[]

  • Homocystinuria

    OBJECTIVE: To describe the long-term ophthalmologic outcomes of patients with methylmalonic aciduria and homocystinuria, cobalamin C type (cblC).[] Long, thin fingers, tall stature, and a high arched palate are seen in some individuals and the hair is often lightly pigmented.[] KEYWORDS: Ectopia lentis; Homocystinuria; Non-traumatic; Pakistan[]

  • Ectopia Lentis

    PURPOSE: To report the clinical features and long-term visual results in children with ectopia lentis after lensectomy.[] […] and tapered, clawlike finger-ends he suggested the present name arachnodactyly ("spider digits").[] Ectopia lentis. Dislocated lens into the vitreous secondary to trauma. Ectopia lentis.[]

  • Congenital Contractural Arachnodactyly

    When severe congenital contractural arachnodactyly is diagnosed in the newborn period, parents need to be aware that long-term survival is possible, particularly if no significant[] fingers and contractures involving the knees, elbows, fingers and sometimes other joints.[] We report on a patient with CCA with bilateral ectopia lentis and aortic root dilatation.[]

  • Goldberg-Shprintzen Syndrome

    Prognosis Little information is available about the long-term outlook for individuals with Goldberg-Schprintzen megacolon syndrome.[] The main features of this condition include a long, thin body type, long fingers and toes, contractures, underdeveloped muscles, “crumpled” ears, and occasionally widening[] […] age 20 years or older [1] Ectopia lentis syndrome Autosomal dominant Ectopia lentis Variable skeletal manifestations reminiscent of the Marfan syndrome Heterozygous mutations[]

  • MASS Syndrome

    These conditions share many of the same signs and symptoms including long limbs and fingers, chest wall abnormalities (indented chest bone or protruding chest bone), flat[] They can include: Abnormal facial appearance Eye problems such as nearsightedness Crowding of teeth Tall, thin body Abnormally shaped chest Long arms, legs, and fingers Laxity[] More than 30 mutations in the FBN1 gene have been found to cause isolated ectopia lentis.[]

  • Disorder of the Lens

    We have recruited staff members dedicated to furthering our mission to reshape systemic issues that inhibit long-term recovery.[] ., long arms, legs and fingers; tall thin body type; curved spine, etc.) together with lens dislocation of the eye, but have no other Marfan features such as those affecting[] . [3] Ocular diseases associated with ectopia lentis Simple ectopia lentis – simple ectopia lentis can occur as a congenital disorder or as a spontaneous disorder later in[]

  • Geleophysic Dysplasia

    […] bone Long bone shortening 0003026 Short metacarpals with rounded proximal ends Short long bone of hand with rounded innermost ends 0006161 Short nose Decreased length of[] She had long upper lip with thin vermillion. Her fingers and toes were short. Her skin was thick, and joint mobility was restricted.[] Weill-Marchesani syndrome, on the basis of microspherophakia and ectopia lentis; geleophysic dysplasia by progressive cardiac valvular thickening, tracheal stenosis, and/or[]

  • Isolated Ectopia Lentis

    Thus, further weakening of the zonules may occur in the long run and, in the most unfortunate cases, may cause luxation of the capsular bag into the vitreous body.[] ., long arms, legs and fingers; tall thin body type; curved spine, etc.) together with lens dislocation of the eye, but have no other Marfan features such as those affecting[] We here describe an isolated form of ectopia lentis in a large inbred family that shows autosomal-recessive inheritance.[]

  • Foveal Hypoplasia - Presenile Cataract Syndrome

    114205 long QT syndrome 8; Brugada syndrome 3 AD 30 CALM1 114180 Ventricular tachycardia, catecholaminergic polymorphic, 4; Long QT syndrome 14 AD 1 CALM2 114182 Long QT[] , spider-like fingers and toes; long, thin arms and legs with a high risk of fracture; pigeon chest or barrel chest; cardiovascular abnormalities, mainly aortic dissecting[] Ectopia lentis may be hereditary or acquired.[]

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