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2,396 Possible Causes for Hypoplasia, Fusion and Contractures of Post-Axial Fingers

Did you mean: Hypoplasia, Fusion and, Contractures, of Post-Axial Fingers

  • Arthrogryposis Multiplex Congenita

    Pathological examination of the brain and spinal cord revealed severe hypoplasia of dorsal roots and posterior columns, nondecussation of pyramidal tracts, and anterior horns[] Nine children had quadrimelic contractures and two had bimelic contractures of the lower limbs (Table 1 ).[] Arthrogryposis multiplex congenita pulmonary hypoplasia Arthrogryposis multiplex congenita pulmonary hypoplasia arthrogryposis multiplex congenita syndrome Arthrogryposis[]

  • Congenital Contractural Arachnodactyly

    […] addition to long fingers and toes and a tall, slender body, people with CCA often have ears that appear to be crumpled, joint stiffness, and underdeveloped muscles (muscular hypoplasia[] Congenital contractural arachnodactyly (Beals syndrome) is an autosomal dominantly inherited connective tissue disorder characterized by multiple flexion contractures, arachnodactyly[] […] is an autosomal-dominant connective tissue disorder characterized by multiple flexion contractures, arachnodactyly, severe kyphoscoliosis, abnormal pinnae, and muscular hypoplasia[]

  • Neurogenic Arthrogryposis Multiplex Congenita

    Arthrogryposis multiplex congenita pulmonary hypoplasia Arthrogryposis multiplex congenita pulmonary hypoplasia arthrogryposis multiplex congenita syndrome Arthrogryposis[] English neurogenic arthrogryposis multiplex congenita congenital joint contracture in two or more areas of the body arthrogryposis multiplex congenita AMC Guérin-Stern syndrome[] Muscle strength does not tend to worsen, however contractures can lead to worsening of function ability.[]

  • Tel Hashomer Camptodactyly Syndrome

    @article{Goodman1976CamptodactylyWM, title {Camptodactyly, with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases: Tel Hashomer camptodactyly syndrome.}[] Although the presence of contractures is specific for CCA, molecularly proven MFS patients with mild contractures have been reported (8).Thus screening for FBN1 and FBN2 genes[] This syndrome is characterized by skeletal dysplasia, muscle hypoplasia, camptodactyly, and abnormal dermatoglyphics.[]

  • Arthrogryposis Syndrome

    MRI brain at the age of 150 days showed hypoplasia of the corpus callosum, with insufficient myelination. Electromyography was consistent with muscular atrophy.[] Contractures of hips, elbows, wrists, and fingers were much milder though they varied in severity among affected individuals.[] […] cholestasis syndrome/ARC Syndrome Arthrogryposis multiplex congenital/Distal type 1 Arthrogryposis multiplex congenita neurogenic type/Arthrogryposis multiplex congenita pulmonary hypoplasia[]

  • Joint Contracture

    All had severe craniosynostosis with midface hypoplasia, elbow joint contracture, developmental retardation, and early death.[] KEYWORDS: Flexor tendon; Interphalangeal joint contracture; Proximal interphalangeal joint contracture; Pulley; Trigger finger; Ultrasonography[] […] diagnoses of Muntaha's condition. 17, 71-73) More severe deformities include MP joint contractures, ulnar collateral ligament laxity, superficial thenar muscle absence or hypoplasia[]

  • Autosomal-Recessive Non-Lethal Multiple Pterygium Syndrome

    , diaphragmatic hernia, obstructive uropathy, microcephaly, or cerebellar and pontine hypoplasia.[] […] multiple pterygium syndrome is a rare distal arthrogryposis syndrome characterized by multiple pterygia (typically involving the neck, axilla and popliteal areas), joint contractures[] This classical syndrome consists of congenital contractures, pterygia (skin webs across joints).[]

  • Isolated optic nerve hypoplasia

    OBJECTIVES: To assess the prevalence of behavioral problems in children with isolated optic nerve hypoplasia, mild to moderate or no visual impairment, and no developmental[] No contractures or hip abnormalities were noted. The bridge of the nose was flat and he appeared to have mild hypertelorism.[] The identification and measurement of autistic features in children with optic nerve hypoplasia, "isolated" hypopituitarism and varying combinations of septo-optic Dysplasia[]

  • Arthrogryposis-Renal Dysfunction-Cholestasis Syndrome

    Hepatic anomalies include variable combinations of cholestasis, intrahepatic biliary duct hypoplasia and lipofuscin deposition.[] The classical presentation of ARC includes congenital joint contractures, renal tubular dysfunction, and cholestasis.[] […] recessive multisystem disorder (OMIM:208085) characterised by neurogenic arthrogryposis multiplex congenita, renal tubular dysfunction and neonatal cholestasis with bile duct hypoplasia[]

  • Oligohydramnios

    Abstract From January 1986 to December 1988, 5 cases of oligohydramnios with pulmonary hypoplasia were experienced.[] Sixty percent (18/30) seemed to have their multiple congenital contractures (MCC) primarily on the basis of compression related to the longstanding oligohydramnios and responded[] BACKGROUND/PURPOSE: Severe neonatal pulmonary hypoplasia incurs mortality rates approaching 71% to 95%.[]

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