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55 Possible Causes for Fetal Finger Pads, Pediatric Disorder

  • Smith-Magenis Syndrome

    finger pads, and polydactyly.[orpha.net] Smith-Magenis Syndrome (SMS) is a complex, pediatric, neurobehavioral, contiguous gene syndrome ascribed to interstitial microdeletion of chromosome 17, band 11.2.[ncbi.nlm.nih.gov] Some cases also show limited elbow-extension span, clinodactyly of the fifth finger, syndactyly of the second and third toes, persistence of fetal pads, and polydactyly.[ojrd.biomedcentral.com]

  • Kabuki Syndrome

    […] congenital disorder of genetic origin.[en.wikipedia.org] finger pads and distinct facial features.[ncbi.nlm.nih.gov] disorder of genetic origin.[senteacher.org]

  • Fetal Erythroblastosis

    Data Cues list assessment data to help you recognize possible pediatric disorders.[books.google.de] […] demise care Fetal heart rate monitoring Fiber-optic phototherapy pads and blankets use, neonate Finger and heel sticks, pediatric Gestational age determination Heat lamp[quizlet.com] Blood disorders. In: Kliegman RM, Stanton BF, St. Geme JW, Schor NF, eds. Nelson Textbook of Pediatrics . 20th ed. Philadelphia, PA: Elsevier; 2016:chap 103.[medlineplus.gov]

  • Microdeletion 3q29 Syndrome

    Mary Coleman is a pediatric neurologist specializing in neurodevelopmental disorders.[books.google.de] The following clinical features are also frequent: fifth finger clinodactyly and small feet/hands, syndactyly of the fingers or toes, persistent fetal finger pads and a single[orpha.net]

  • Pitt-Hopkins Syndrome

    People with PTHS can have particularly fleshy pads in the tips of their fingers or toes.These are known as fetal pads. Short sightedness or a squint. Undescended testes.[pitthopkins.org.uk] Iossifov I , et al. (2015) Yes - 18 Support Next-generation sequencing using a pre-designed gene panel for the molecular diagnosis of congenital disorders in pediatric patients[gene.sfari.org] Other features include a single (simian) palmar crease, long, slender fingers, flat feet and cryptorchidism (in males). The presence of fetal pads is common.[en.wikipedia.org]

  • LEOPARD Syndrome

    finger pads (lumps on fingertips; see photos below) Atrial or ventricular septal defects Wide chest/widely spaced nipples Undescended testicles in boys Hypertrophic cardiomyopathy[forgottendiseases.org] […] symptoms in infants, children, and young adults through images of common and unusual presenting features for over 300 pediatric disorders.[euro-libris.ro] Disorders of pigmentation. In: Paller AS, Mancini AJ, eds. Hurwitz Clinical Pediatric Dermatology. 5th ed. Philadelphia, PA: Elsevier; 2016:chap 11.[medlineplus.gov]

  • Chromosome 15q26-Qter Deletion Syndrome

    […] microcephaly monosomy MTHFR myelomeningocele Nat Genet neural tube defects NTD risk NTDs Obstet Gynecol occipital encephalocele OEIS complex OMIM omphalocele palate patients Pediatr[books.google.de] The following clinical features are also frequent: fifth finger clinodactyly and small feet/hands, syndactyly of the fingers or toes, persistent fetal finger pads and a single[orpha.net] Autosomal ring chromosomes in human genetic disorders. Transl Pediatr 2015;4(2):164-174. doi: 10.3978/j.issn.2224-4336.2015.03.04[tp.amegroups.com]

  • Rubinstein-Taybi Syndrome

    […] persistent fetal pads, clinodactyly of the fifth fingers skull and central nervous system microcephaly mental retardation (IQ 35-50) congenital cardiac abnormalities: reported[radiopaedia.org] Pediatr Dermatol. 1994; 11(1):21-5 [ PubMed ] Related Publications Rubinstein-Taybi syndrome is a multisystem developmental disorder due to an autosomal dominant mutation.[cancerindex.org] Med Pediatr Oncol 1989, 17: 485–91. View Article PubMed Google Scholar Copyright Bounakis et al.; licensee BioMed Central. 2015[jmedicalcasereports.com]

  • Legius Syndrome

    finger pads (lumps on fingertips; see photos below) Atrial or ventricular septal defects Wide chest/widely spaced nipples Undescended testicles in boys Hypertrophic cardiomyopathy[forgottendiseases.org] Legius syndrome is one of the RASopathies, which are a class of pediatric disorders associated with genes that are members of the mitogen-activated protein kinase (Ras/ MAPK[invitae.com] Frieden, two of the most important names in the fields of dermatology and pediatrics.[books.google.com]

  • X-Linked Mental Retardation 93

    Other signs and symptoms include physical and neurological features as follows: Common clinical features of Kabuki syndrome Fetal finger pads (lumps on fingertips; see photos[forgottendiseases.org] Pediatrics 82:582-95) Hospital admissions 11.1% of pediatric hospital admissions are for children with genetic disorders and 18.5% are children with other congenital malformations[kumc.edu] Child psychiatric disorders and their correlates: A primary care pediatric sample. Journal of the American Academy of Child and Adolescent Psychiatry, 28 851–855.[link.springer.com]

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