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1,785 Possible Causes for Anterior Fontanelle Open in Adults, Multiple Congenital Anomalies

  • Cleidocranial Dysplasia

    Abstract Cleidocranial dysplasia (CCD) is an autosomal dominant skeletal disorder exhibiting a wide clinical spectrum ranging from minimal anomalies to classic CCD. Mutations scattered throughout the entire CBFA1 gene have been related to this disorder. However, it seems that most of them affect the highly conserved[…][ncbi.nlm.nih.gov]

  • Patau Syndrome

    Trisomy 13 or Patau syndrome (PS) is a chromosomal disorder characterized by a well known presentation of multiple congenital anomalies.[ncbi.nlm.nih.gov] congenital anomalies.[genome.jp] Wagner: Multiple congenital anomaly caused by an extra autosome. The Lancet, London, 1960, I: 790. What is an eponym?[whonamedit.com]

    Missing: Anterior Fontanelle Open in Adults
  • Winchester Syndrome

    This group will include 50% with chromosomal disorders congenital anomaly syndromes, especially recognizable by performing a karyotype, the details about their features and[books.google.de] Both the database and this malformation, but in the region of 8 in 1000 book have arisen out of a need to cope with the ever increasing nurober of multiple will have multiple[books.google.de]

    Missing: Anterior Fontanelle Open in Adults
  • Pierre Robin Syndrome

    Keywords Patau syndrome trisomy 13 multiple congenital anomalies Pierre Robin syndrome metabolic abnormalities fluorescence in situ hybridization DNA-microarray This is a[doi.org] Keywords Pierre robin syndrome; Mobius syndrome; Palatoglossal fusion; Fiberoptic intubation Introduction Pierre Robin Syndrome (PRS) is a congenital syndrome with multiple[omicsonline.org] Anaesth Pain & Intensive Care 2013;17(1):71-74 INTRODUCTION Pierre Robin Syndrome (PRS) is a congenital syndrome, consisting of multiple anomalies, including, micrognathia[apicareonline.com]

    Missing: Anterior Fontanelle Open in Adults
  • Mucopolysaccharidosis

    Urology. 2017 Mar;101:163-165. doi: 10.1016/j.urology.2016.12.010. Epub 2016 Dec 20. Author information 1 Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Higashi-ku, Fukuoka, Japan. Electronic address: nkei@pediatr.med.kyushu-u.ac.jp. 2 Department of Pediatrics, Graduate School of Medical[…][ncbi.nlm.nih.gov]

    Missing: Anterior Fontanelle Open in Adults
  • Turner Syndrome

    Cardiovascular anomalies are common and the most clinically frequent is coarctation of the aorta.[magicfoundation.org] […] arched palate, micrognathia, broad chest, cubitus valgus, multiple pigmented nevus, abnormal finger nails, intestinal telangiectasia and hypoplastic nipples.[magicfoundation.org] Characteristics Children with Turner's Syndrome may have the following physical findings; congenital lymphedema, low posterior hair line, webbed neck, prominent ears, high[magicfoundation.org]

    Missing: Anterior Fontanelle Open in Adults
  • Crouzon Syndrome

    CONGENITE MULTIPLE CON RITARDO MENTALE RP0040 SINDROME ALCOLICA FETALE[webalice.it] 11 classification [BR: br08403 ] 20 Developmental anomalies Multiple developmental anomalies or syndromes LD24 Syndromes with skeletal anomalies as a major feature H01754[genome.jp] More specifically, however, the term has come to imply congenital deformities of the head that interfere with physical and mental well-being. [1] Most craniofacial anomalies[jdrntruhs.org]

    Missing: Anterior Fontanelle Open in Adults
  • Craniosynostosis

    Noonan syndrome (NS) is a multiple congenital anomaly syndrome caused by germline mutations in genes coding for components of the Ras-mitogen-activated protein kinase (RAS-MAPK[ncbi.nlm.nih.gov] There are forms of craniosynostosis that are part of an inherited syndrome and associated with a host of congenital anomalies.[medlink.com] These syndromes usually involve multiple sutures, especially the coronal. Nonsyndromic craniosynostosis, an isolated birth defect, is usually sporadic.[medlink.com]

    Missing: Anterior Fontanelle Open in Adults
  • Fraser Syndrome

    She had multiple congenital anomalies which included a cardiac defect and airway abnormalities.[ncbi.nlm.nih.gov] Cryptophthalmos refers to a group of uncommon congenital anomalies of eyelid formation that can occur alone or in combination with multiple congenital anomalies as part of[ncbi.nlm.nih.gov] Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes. National Library of Medicine. nd. 2pp. www.nlm.nih.gov/mesh/jablonki/syndromes/syndrome302.html[rarediseases.org]

    Missing: Anterior Fontanelle Open in Adults
  • Russell-Silver Syndrome

    congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome, malformation syndrome with short stature, polymalformative genetic syndrome with increased[commons.wikimedia.org] […] in ICD-11 classification [BR: br08403 ] 20 Developmental anomalies Multiple developmental anomalies or syndromes LD2F Syndromes with multiple structural anomalies, without[genome.jp] […] file multimediale Wikipedia Istanza di malattia, difetto dello sviluppo durante l'embriogenesi Sottoclasse di chromosomal disease, nanismo primordiale, inherited tumor, multiple[commons.wikimedia.org]

    Missing: Anterior Fontanelle Open in Adults

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