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1,064 Possible Causes for Focal Keratoderma of Soles, Maxillary Hypoplasia

  • Growth Hormone Deficiency

    Palmoplantar keratoderma (PPK) is a diverse group of disorders, characterized by thickening of the palms and soles, which are subdivided into focal or diffuse; it can be acquired[ncbi.nlm.nih.gov] In children suffering from significant GH deficiency the facial features are distinguished by a prominence of the forehead and maxillary hypoplasia.[hgh.org] Some severely GH-deficient children have recognizable, cherubic facial features characterized by maxillary hypoplasia and forehead prominence (said to resemble a kewpie doll[en.wikipedia.org]

  • Crouzon Syndrome

    Crouzon syndrome is an autosomal dominant genetic disease characterized by bicoronal craniosynostosis, exorbitism with hypertelorism, and maxillary hypoplasia with mandibular[ncbi.nlm.nih.gov] Crouzon syndrome is a craniostenotic craniofacial malformation associated with premature closure of selective calvarial sutures, exophthalmos, maxillary hypoplasia, and a[ncbi.nlm.nih.gov] Orofacial manifestations of this disease include maxillary hypoplasia, external nasal deformity, and prognathism.[ncbi.nlm.nih.gov]

    Missing: Focal Keratoderma of Soles
  • Rieger Syndrome

    At presentation, typical components of ARS could be found in both patients, including iris anomaly, maxillary hypoplasia, hypodontia, and umbilical skin fold.[ncbi.nlm.nih.gov] Synonym(s): iridocorneal mesodermal dysgenesis Rieger syndrome - Rieger anomaly combined with hypodontia or anodontia and maxillary hypoplasia.[medical-dictionary.thefreedictionary.com] These patients might have a difficult airway due to facial anomalies, brachycephaly and maxillary hypoplasia.[aeronline.org]

    Missing: Focal Keratoderma of Soles
  • Axenfeld-Rieger Syndrome Type 3

    Systemic anomalies include craniofacial dysmorophisms such as hypertelorism, telecanthus, maxillary hypoplasia, and a broad, flat nasal bridge.[webeye.ophth.uiowa.edu] Diagnosis is best made by ruling out mutations in PITX1 and FOXC1 although it is claimed that maxillary hypoplasia and umbilical defects are less common in type 2.[disorders.eyes.arizona.edu] Anomalies include anterior segment dysgenesis of the eye, dental anomalies, maxillary hypoplasia, periumbilical anomalies, and congenital heart defects.[karger.com]

    Missing: Focal Keratoderma of Soles
  • Autosomal Dominant Prognathism

    Hartsfield Abstract Often referred to as mandibular prognathism, the Class III phenotype can be a result of mandibular prognathism, maxillary hypoplasia (also termed maxillary[ebooks.benthamscience.com]

    Missing: Focal Keratoderma of Soles
  • Apert Syndrome

    A concave profile and a skeletal Class III jaw-base relationship caused by severe maxillary hypoplasia were seen in all patients.[ncbi.nlm.nih.gov] Apert syndrome is characterised by craniosynostosis, associated with maxillary hypoplasia, symmetrical syndactyly of the hands and feet, and other systemic malformations including[ncbi.nlm.nih.gov] Apert syndrome is a congenital condition characterized by craniosynostosis, syndactyly, and maxillary hypoplasia.[ncbi.nlm.nih.gov]

    Missing: Focal Keratoderma of Soles
  • Stomatitis

    Turner's hypoplasia Enamel pearl Fluorosis Fusion Gemination Hyperdontia Hypodontia Maxillary lateral incisor agenesis Impaction Wisdom tooth impaction Macrodontia Meth mouth[en.wikipedia.org] […] bite abnormalities Bruxism Condylar resorption Mandibular dislocation Malocclusion Crossbite Open bite Overbite Overeruption Overjet Prognathia Retrognathia Scissor bite Maxillary[en.wikipedia.org] hypoplasia Temporomandibular joint dysfunction Salivary glands Benign lymphoepithelial lesion Ectopic salivary gland tissue Frey's syndrome HIV salivary gland disease Necrotizing[en.wikipedia.org]

    Missing: Focal Keratoderma of Soles
  • Aarskog Syndrome

    Primary criteria include: short stature, hypertelorism, short nose with anteverted nares, maxillary hypoplasia, a crease below the lower lip, mild interdigital webbing with[ncbi.nlm.nih.gov] hypoplasia, hypodontia, retarded dental eruption, orthodontic problems 3.[web.archive.org] hypoplasia and transverse crease below the lower lip.[orpha.net]

    Missing: Focal Keratoderma of Soles
  • Gingivitis

    Turner's hypoplasia Enamel pearl Fluorosis Fusion Gemination Hyperdontia Hypodontia Maxillary lateral incisor agenesis Impaction Wisdom tooth impaction Macrodontia Meth mouth[en.wikipedia.org] […] bite abnormalities Bruxism Condylar resorption Mandibular dislocation Malocclusion Crossbite Open bite Overbite Overeruption Overjet Prognathia Retrognathia Scissor bite Maxillary[en.wikipedia.org] hypoplasia Temporomandibular joint dysfunction Salivary glands Benign lymphoepithelial lesion Ectopic salivary gland tissue Frey's syndrome HIV salivary gland disease Necrotizing[en.wikipedia.org]

    Missing: Focal Keratoderma of Soles
  • Gorlin-Chaudhry-Moss Syndrome

    Craniofacial malformations are present, such as midface hypoplasia, and maxillary hypoplasia (difficult tracheal intubation).[accessanesthesiology.mhmedical.com] Maxillary hypoplasia can be a cause for the dental particularities. Close attention must be paid to the examination of the extremities.[symptoma.com] Radiological features include premature synostosis of the coronal suture, brachycephaly, and maxillary under-development.[ncbi.nlm.nih.gov]

    Missing: Focal Keratoderma of Soles

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