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144 Possible Causes for Hypertrichosis of Eyebrows, Pediatric Disorder

  • Fucosidosis

    Pediatr Radiol 2007;37:1050-2. 8. Sanklecha MU, Kher A, Naik GG, Bharucha BA, Mahajan P. Storage disorders presenting like mucopolysaccharidosis.[pediatricneurosciences.com] Center for Human Genetics and is Director of the Rare Brain Disorders Program (Clinic and Laboratory).[books.google.de] J Pediatr Neurosci 2014;9:156-8 Fucosidosis is a rare lysosomal storage disorder, which is inherited in autosomal recessive pattern due to deficient activity of the enzyme[pediatricneurosciences.com]

  • Alpha-Mannosidosis

    Disorders E-2903 168 Measurement of Health Outcomes in Pediatric Neurologic Disorders E-2910 169 The Influence of Computer Resources on Child Neurology E-2918 170 Education[books.google.es] Pediatrics, 114, 909-916. [2] Meikle, P., Hopwood, J., Clague, A., & Carey, W. (1999). Prevalence of lysosomal storage disorders.[oncofertility.northwestern.edu] Lysosomal storage disorders in the newborn. Pediatrics . 2009 Apr. 4:1191-207. [Medline] . [Full Text] . Uz E, Cipil H, Turgut FH, Kaya A, Kargili A, Bavbek N, et al.[emedicine.medscape.com]

  • SHORT Syndrome

    Pediatric disorders of sex development. In: Melmed S, Polonsky KS, Larsen PR, Kronenberg HM, eds. Williams Textbook of Endocrinology. 13th ed.[medlineplus.gov] We and others noticed that some patients had features reminiscent of CdLS, particularly where facial hypertrichosis and prominent eyebrows were present.[nature.com] Nelson textbook of pediatrics. 1. 20th ed. Philadelphia: Elsevier; 2016.p. 84-9. [ Links ] 5 Ergun-Longmire B, Wajnrajch MP. Growth and growth disorders.[scielo.br]

  • Klein-Waardenburg Syndrome

    Frieden, two of the most important names in the fields of dermatology and pediatrics.[books.google.de] […] of the medial part of the eyebrows, (4) white forelock, (5) heterochromia iridis, and (6) deaf-mutism.[medlink.com] Shah, et al: White forelock, pigmentary disorder of irides, and long segment Hirschprung disease: Possible variant of Waardenburg syndrome. Journal of Pediatrics, St.[whonamedit.com]

  • Beckwith-Wiedemann Syndrome

    Beckwith-Wiedemann syndrome (BWS) is a pediatric overgrowth disorder involving a predisposition to tumor development, including adrenal lesions.[ncbi.nlm.nih.gov] […] nasal bridge, hypoplastic philtrum and prominent jaw, low posterior hairline, and hypertrichosis.[ncbi.nlm.nih.gov] Beckwith-Wiedemann syndrome is a pediatric overgrowth disorder.[patientslikeme.com]

  • Thanatophoric Dysplasia

    .: Thanatophoric dysplasia type I: new radiologic, morphologic, and histologic aspects toward the exact definition of the disorder. J Pediatr Orthop B 7:1–9, 1998.[link.springer.com] […] lungs Cloverleaf skull Feeding difficulties in infancy Rare Symptoms - Less than 30% cases Smooth philtrum Hypoglycemia Talipes Hyperhidrosis Mandibular prognathia Thick eyebrow[mendelian.co] Explore the impact of today’s advances and challenges, including explosive growth in molecular biology, sophisticated imaging techniques, and an increase in both pediatric[books.google.com]

  • Wiedemann-Steiner Syndrome

    Previously: A look at one woman's long journey to diagnosis and treatment of a rare disorder , Developing a Google-like search system to improve diagnosis, treatment of pediatric[scopeblog.stanford.edu] […] cubiti, facial dysmorphism (hypertelorism, long eyelashes, thick eyebrows, downslanted, vertically narrow, long palpebral fissures, wide nasal bridge, broad nasal tip, long[orpha.net] Previously: A look at one woman's long journey to diagnosis and treatment of a rare disorder, Developing a Google-like search system to improve diagnosis, treatment of pediatric[scopeblog.stanford.edu]

  • Rubinstein-Taybi Syndrome

    Author information 1 Department of Pediatrics, Emma's Children's Hospital/Academic Medical Center, Amsterdam, The Netherlands.[ncbi.nlm.nih.gov] The clinical data of our cohort evidenced frequent signs such as arched eyebrows, epicanthus, synophrys and/or frontal hypertrichosis and broad phalanges that, previously[ncbi.nlm.nih.gov] The common abnormalities include hypertrichosis and hirsuitism,heavy eyebrows, prominent beaked nose,hypoplastic maxilla, lowest ears and skeletal anomalies including broad[ispub.com]

  • Marshall-Smith Syndrome

    Smith: Syndrome of accelerated skeletal maturation and relative failure to thrive: A newly recognized clinical growth disorder. Journal of Pediatrics, St.[whonamedit.com] Syndrome of accelerated skeletal maturation and relative failure to thrive: a newly recognized clinical growth disorder.[ncbi.nlm.nih.gov] A dominantly inherited disorder with normal intelligence. Journal of Pediatrics, St. Louis, 1970, 77: 129-133. R. E. Marshall, C. B. Graham, C. R.[whonamedit.com]

  • Cerebro-Facio-Thoracic Dysplasia

    TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities. Am J Hum Genet 93:197-210.[bhcmg.org] ), a narrow forehead and a short nose; there are also hypertrichosis (espec- ially posteriorly) and mental retardation.[vdocuments.site] This study supports the fact that "TMCO1-defect syndrome," initially thought to represent a distinct disorder, indeed belongs to the genetically heterogeneous CFT dysplasia[unboundmedicine.com]

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