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3,759 Possible Causes for Bilateral Clinodactyly, Failure to Thrive, Urine Hyaluronic Acid Increased

  • Ruijs Aalfs Syndrome

    In addition, he had thoracic kyphoscoliosis, sloping shoulders, mild pectus excavatum, moderate bilateral contractures of both elbows, bilateral clinodactyly, and pes planus[] […] to thrive, sinus disease, and respiratory disease [ 36 ].[] […] functions as an ion channel involved in the transport of chloride and thiocyanate and is associated with cystic fibrosis, a condition manifested by pancreatic insufficiency, failure[]

  • Growth Failure

    There was bilateral clinodactyly (an incurved fifth finger) and a single palmar crease in the left hand.[] Presentation on theme: "Faltering growth(failure to thrive)"— Presentation transcript: 1 Faltering growth(failure to thrive) refers to not only failure of growth(suboptimal[] […] of II left digit and V digit bilaterally, feet with broad big toes, brachydactyly, and left clubfoot (Figure 1C,D).[]

    Missing: Urine Hyaluronic Acid Increased
  • Pierre Robin Syndrome

    A nine day old boy who had the Pierre Robin syndrome also had an unusual associated hand malformation consisting of bilateral clinodactyly of the index finger.[] This failure to thrive was reversed in the infants managed with NP tubes in comparison with an age-matched groups nursed while prone.[] Two patients then improved dramatically; whereas one continued with respiratory distress and failure to thrive and required tracheostomy.[]

    Missing: Urine Hyaluronic Acid Increased
  • Juvenile Cystinosis

    [Table/Fig-1]: Short stature in compared with the child of same age Other findings on examination include frontal bossing, pallor, bilateral clinodactyly, short fourth metatarsals[] Failure to thrive is generally noticed after approximately age six months; signs of renal tubular Fanconi syndrome (polyuria, polydipsia, dehydration, and acidosis) appear[] The disease results in deposition of crystals throughout the body; if untreated, it leads to failure to thrive, profound metabolic imbalance, early end-stage renal disease[]

    Missing: Urine Hyaluronic Acid Increased
  • Russell-Silver Syndrome

    clinodactyly.[] Russell-Silver syndrome is characterized by asymmetric intrauterine growth retardation, postnatal failure to thrive, distinct facial features, limb asymmetry, excessive sweating[] Mosaic trisomy 7 was diagnosed after birth, on fibroblasts karyotype performed for blaschkolinear pigmentary skin anomalies and failure to thrive.[]

    Missing: Urine Hyaluronic Acid Increased
  • Smith Lemli Opitz Syndrome

    He also had two-to-three toe syndactyly bilaterally ( Figure 2 ) and curving of the little finger toward the fourth finger (clinodactyly) bilaterally.[] Affected individuals have dysmorphism, short stature, failure to thrive, microcephaly, multiple congenital malformations, and mental retardation.[] Genetically and clinically heterogeneous disorder characterized by low birth weight, postnatal growth retardation, facial dysmorphism, bilateral body asymmetry, and clinodactyly[]

    Missing: Urine Hyaluronic Acid Increased
  • Marshall-Smith Syndrome

    […] of the fifth finger on both hands and bilateral hallux valgus.[] It is hoped that the etiology of the syndrome will be discovered as more cases are recognized and reported by pediatricians caring for infants with failure to thrive, advanced[] Marshall A syndrome of motor and mental retardation, accelerated skeletal maturation, failure to thrive, and abnormal facies.[]

    Missing: Urine Hyaluronic Acid Increased
  • Wolf-Hirschhorn Syndrome

    Systemic findings included "Greek warrior helmet" facies, hypotonia, cleft palate, neonatal tooth eruption, talipes equinovarus, bilateral clinodactyly, clitoromegaly, partial[] Accordingly, prenatal-onset growth retardation and failure to thrive have been found to result from haploinsufficiency for a 4p gene located between 0.4 and 1.3 Mb, whereas[] Clinical manifestations of WHS include intrauterine growth restriction, failure to thrive in the neonatal period that is present simultaneously with hypotonia, typical "Greek[]

    Missing: Urine Hyaluronic Acid Increased
  • Fanconi Renotubular Syndrome

    He had prominent facial veins, sparse hair, thin skin, abnormal eye movement, and bilateral clinodactyly [Figure 1].[] Main clinical findings are polyuria, failure to thrive, rickets/osteomalacia, metabolic acidosis, bone deformities, and, occasionally, nephrocalcinosis.[] Symptoms in children are failure to thrive, growth retardation, and rickets. Symptoms in adults are osteomalacia and muscle weakness.[]

    Missing: Urine Hyaluronic Acid Increased
  • Ring Chromosome 9

    clinodactyly.[] An eight-mth-old boy, presenting with broad and dark eyebrows with protruding tongue, microcephaly, short stature and failure to thrive was found to have ring chromosome 9[] […] to thrive beyond the extent expected from their chromosomal imbalances (Kosztolanyi 1987). suggested that this is due to the mitotic instability of rings, preventing somatic[]

    Missing: Urine Hyaluronic Acid Increased

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