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40 Possible Causes for Fetal Finger Pads, Pediatric Disorder

  • Smith-Magenis Syndrome

    Abstract 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] finger pads, and polydactyly.[orpha.net] J Dev Behav Pediatr. 2006 Jun;27(3):188-92. Neira-Fresneda J, Potocki L.[ghr.nlm.nih.gov]

  • 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] […] tips and wide and flat palate Broad finger tips and wide and flat palate Strabismus, scoliosis, sacral dimple, fetal finger pads, overriding 5th toe, and short metatarsal[ncbi.nlm.nih.gov]

  • Kabuki Syndrome

    finger pads and distinct facial features.[ncbi.nlm.nih.gov] Kabuki syndrome (KS) is a rare pediatric congenital disorder with multiple congenital anomalies and intellectual disabilities, which is inherited in an autosomal dominant[ncbi.nlm.nih.gov] disorder of genetic origin.[senteacher.org]

  • Eye Muscle Disorder

    […] or vertebrae; persistent finger fetal pads, mild to moderate intellectual disability; and short stature.[apraxia-kids.org] Charlotte Thompson, a leading authority in pediatric neuromuscular disorders, draws on her 38 years of experience treating children with muscular dystrophy, spinal atrophy[books.google.com] It also may accompany a number of eye disorders and neurological disorders.[dmei.org]

  • 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] Author information 1 Department of Pediatrics, Emma's Children's Hospital/Academic Medical Center, Amsterdam, The Netherlands.[ncbi.nlm.nih.gov] Terminal broadening of the phalanges of the fingers, persistent fetal pads, clinodactyly of the fifth finger, overlapping of the toes, and angulation deformities of the thumbs[ommbid.mhmedical.com]

  • Goldberg-Shprintzen Syndrome

    Additional dysmorphic features may include maxillary hypoplasia, hypodontia, high arched palate, short neck, small hands, brachydactyly, fifth finger clinodactyly, fetal finger[orpha.net] Dismiss this warning Case report and review of the literature View More View Less Departments of Neurosurgery, Pediatric Neurology and Epileptology, and Pediatric Radiology[thejns.org] pads and flatfoot.[orpha.net]

  • Legius Syndrome

    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] 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] Frieden, two of the most important names in the fields of dermatology and pediatrics.[books.google.com]

  • Mowat-Wilson Syndrome

    […] joints) and Kabuki syndrome (persistent fetal fingertip pads).[childnervoussystem.blogspot.com] Jose Garza is Logan's pediatric gastroenterologist, "He's a great kid," Dr. Garza says.[fox5atlanta.com] The hands provide specific clues in Coffin–Lowry syndrome (short, soft hands with hyperextensible joints and tapering fingers), Nicolaides–Baraitser syndrome (prominent interphalangeal[childnervoussystem.blogspot.com]

  • Baraitser-Winter Syndrome 1

    Fetal pads as a clue to the diagnosis of Pitt-Hopkins syndrome. Am J Med Genet A. Jul;155A(7):1685-9.33. 34. Payne M, Rupar CA, Siu GM and Siu VM (2011).[lhsc.on.ca] The thoroughly updated Fourth Edition of this acclaimed reference describes and illustrates the full range of pediatric disorders diagnosable by modern neuroimaging.[books.google.de] NS 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 ) pathway.[invitae.com]

  • Chromosome 15q26-Qter Deletion Syndrome

    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] […] 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] Prenat Diagn prenatal diagnosis renal reported prenatal diagnosis Risk Factors Associated risk of NTDs sacral Sacrococcygeal teratoma sonographic spina bifida Syndromes and Disorders[books.google.de]

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