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18 Possible Causes for Hypertelorism, Mild Maxillary Prognathism

  • Saethre-Chotzen Syndrome

    Chotzen, German psychiatrist, 20th century an autosomal-dominant disorder characterized by acrocephalosyndactyly in which the syndactyly is mild and by hypertelorism, ptosis[medical-dictionary.thefreedictionary.com] The leptoprosopic flat face with mild maxillary hypoplasia and relative mandibular prognathism was exemplified by a prominent chin [ Figure 2 ].[ncbi.nlm.nih.gov] Clinical features of this syndrome include unilateral or bilateral coronal synostosis, ptosis, low-set ears, hearing loss, hypertelorism, maxillary hypoplasia, deviated nasal[ncbi.nlm.nih.gov]

  • Rieger Syndrome

    An ARS variant has been described in two familial cases of Axenfeld-Rieger Anomaly (ARA) featuring specific extra ocular manifestations-hypertelorism, midface hypoplasia,[ncbi.nlm.nih.gov] Facies: - Maxillary hypoplasia - Mild prognathism ... Teeth: - Microdontia - Hypodontia - Cone - shaped teeth ... Ear: - Abnormal ear ... Abdomen: - Umbilical hernia ...[ibis-birthdefects.org] The affected members in family 2 had posterior embryotoxon and iris hypoplasia with early-onset glaucoma, and systemically they had hearing loss, hypertelorism, and telecanthus[ncbi.nlm.nih.gov]

  • Familial Scaphocephaly Syndrome

    Definition An autosomal dominant craniosynostosis syndrome characterized by scaphocephaly, macrocephaly, hypertelorism, maxillary retrusion, and mild intellectual disability[uniprot.org] Note maxillary hypoplasia, ocular proptosis with mild relative prognathism. (From Renier et al. 2000) syndrome is genetically heterogeneous.[rrnursingschool.biz] […] death: - Type of inheritance: autosomal dominant External references: 1 OMIM reference - No MeSH references Very frequent - Autosomal dominant inheritance - High forehead - Hypertelorism[csbg.cnb.csic.es]

  • Axenfeld-Rieger Syndrome Type 3

    Features include posterior corneal embryotoxon, prominent Schwalbe line and iris adhesion to the Schwalbe line, hypertelorism, hypodontia, sensorineural deafness, redundant[uniprot.org] They include mild dysmorphism (hypertelorism, broad flat nose, maxillary hypoplasia, and mild prognathism), dental anomalies (microdontia, hypodontia, anodontia, oligodontia[glaucomatoday.com] Axenfeld-Rieger syndrome Symptoms of Axenfeld-Rieger syndrome type 3 Clinical features : Imported from Human Phenotype Ontology (HPO) Abnormality of head or neck Concave nasal ridge Hypertelorism[familydiagnosis.com]

  • Craniosynostosis Type 3

    Disease description A craniosynostosis syndrome characterized by coronal synostosis, brachycephaly, low frontal hairline, facial asymmetry, hypertelorism, broad halluces,[uniprot.org] Note maxillary hypoplasia, ocular proptosis with mild relative prognathism. (From Renier et al. 2000) syndrome is genetically heterogeneous.[rrnursingschool.biz] - 3 Features -Turribrachycephaly/ Kleeblattschadel -BROAD thumbs or great toes -Midface hypoplasia - BEAK nose -Mild cutaneous syndactyly -Class III malocclusion -Ocular hypertelorism[quizlet.com]

  • Isolated Trigonocephaly

    Orbital hypertelorism. II. Definite treatment of orbital hypertelorism by craniofacial or by extracranial osteotomies.[nature.com] Note maxillary hypoplasia, ocular proptosis with mild relative prognathism. (From Renier et al. 2000) syndrome is genetically heterogeneous.[rrnursingschool.biz] The most common syndromes with hypertelorism are the median cleft syndrome (hypertelorism, median cleft lip with or without a median cleft of the hard palate and nose, and[sonoworld.com]

  • Baller-Gerold Syndrome

    Eyes: Hypertelorism. Nose: Prominent nasal bridge, long philtrum, and epicanthal folds. Mouth and oral structures: Cleft palate, bifid uvula, and highly arched palate.[whonamedit.com] Note maxillary hypoplasia, ocular proptosis with mild relative prognathism. (From Renier et al. 2000) syndrome is genetically heterogeneous.[rrnursingschool.biz] Other distinctive facial features can include widely spaced eyes ( hypertelorism ), a small mouth, and a saddle-shaped or underdeveloped nose.[ghr.nlm.nih.gov]

  • Micrognathism

    Hypertelorism. Delayed ossification of bones forming symphysis pubis, producing a widened symphysis.[findzebra.com] […] of the teeth -Mild prognathism www.indiandentalacademy.com 19.  Hypoparathyroidism - retarded eruption -early exfoliation -enamel defects  Hyperparathyroidism - demineralization[slideshare.net] Syndromic facies and keratosis pilaris Hypertelorism, downward slanting palpebral fissures, micrognathia, ptosis and short neck The echocardiography demonstrated dilatation[ncbi.nlm.nih.gov]

  • Robinow-Sorauf Syndrome

    Related phenotypes are malar flattening and hypertelorism[malacards.org] The leptoprosopic flat face with mild maxillary hypoplasia and relative mandibular prognathism was exemplified by a prominent chin [Figure 2] .[ijdentistry.com] UniProtKB/Swiss-Prot : 75 Robinow-Sorauf syndrome: An autosomal dominant syndrome characterized by craniosynostosis, asymmetry of orbits, flat face, hypertelorism, a thin,[malacards.org]

  • Eyebrow Duplication - Syndactyly Syndrome

    The leptoprosopic flat face with mild maxillary hypoplasia and relative mandibular prognathism was exemplified by a prominent chin [Figure 2].[ijdentistry.com] , high forehead, hypertelorism, slight downslanting palpebral fissures, pale highly arched eyebrows, distinct mouth with thin lips and downturned corners, high narrow palate[chr7.org] Acrocephalosyndactylies, Type III Acrocephalosyndactylies, Acrocephaly-Skull Asymmetry-Mild Syndactyly, Craniofacial-Skeletal-Dermatologic Dysplasia, Dysostosis Craniofacialis with Hypertelorism[xpertdox.com]

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