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14 Possible Causes for Dysmorphic Face, Mild Maxillary Prognathism

  • Saethre-Chotzen Syndrome

    The leptoprosopic flat face with mild maxillary hypoplasia and relative mandibular prognathism was exemplified by a prominent chin [ Figure 2 ].[ncbi.nlm.nih.gov] Crouzon craniofacial dysostosis (OMIM 123500) involves only the face and skull.[rrnursingschool.biz] maxillary hypoplasia and relative mandibular prognathism exemplified by a prominent, wide root of the nose, thick eyebrows, prominent eyelashes, mild convergent strabismus[ncbi.nlm.nih.gov]

  • Micrognathism

    […] of the teeth -Mild prognathism www.indiandentalacademy.com 19.  Hypoparathyroidism - retarded eruption -early exfoliation -enamel defects  Hyperparathyroidism - demineralization[slideshare.net] face is mandatory, associated to another major criteria or two minor criteria.[ncbi.nlm.nih.gov] Symptoms INHERITANCE: Autosomal dominant HEAD AND NECK: [Head]; Plagiocephaly; [Face]; Broad forehead; [Ears]; Dysmorphic ears; [Eyes]; Hypertelorism; [Mouth]; Cleft palate[findzebra.com]

  • Axenfeld-Rieger Syndrome Type 3

    They include mild dysmorphism (hypertelorism, broad flat nose, maxillary hypoplasia, and mild prognathism), dental anomalies (microdontia, hypodontia, anodontia, oligodontia[glaucomatoday.com] The most characteristic non-ocular findings are mild craniofacial dysmorphism, dental anomalies and redundant periumblical skin.[orpha.net] Mid-face abnormalities include hypertelorism, telecanthus, maxillary hypoplasia with flattening of the mid-face, prominent forehead, and broad, flat nasal bridge.[orpha.net]

  • Rieger Syndrome

    Facies: - Maxillary hypoplasia - Mild prognathism ... Teeth: - Microdontia - Hypodontia - Cone - shaped teeth ... Ear: - Abnormal ear ... Abdomen: - Umbilical hernia ...[ibis-birthdefects.org] The most characteristic non-ocular findings are mild craniofacial dysmorphism, dental anomalies and redundant periumblical skin.[orpha.net] They include mild dysmorphism (hypertelorism, broad flat nose, maxillary hypoplasia, and mild prognathism), dental anomalies (microdontia, hypodontia, anodontia, oligodontia[glaucomatoday.com]

  • Craniosynostosis Type 3

    Note maxillary hypoplasia, ocular proptosis with mild relative prognathism. (From Renier et al. 2000) syndrome is genetically heterogeneous.[rrnursingschool.biz] It can include: long narrow face with facial dysmorphisms, congenital cataract, blepharophimosis, dental anomalies, syndactyly, cardiopathy, cleft palate, renal and genital[bredagenetics.com] Crouzon craniofacial dysostosis (OMIM 123500) involves only the face and skull.[rrnursingschool.biz]

  • Isolated Trigonocephaly

    Note maxillary hypoplasia, ocular proptosis with mild relative prognathism. (From Renier et al. 2000) syndrome is genetically heterogeneous.[rrnursingschool.biz] Crouzon craniofacial dysostosis (OMIM 123500) involves only the face and skull.[rrnursingschool.biz] The distinguishing dysmorphism consists in underdevelopment of the midfacial bones, resulting in shallow orbits with ex-ophthalmos, and prognathism with inverted dental occlusion[rrnursingschool.biz]

  • Familial Scaphocephaly Syndrome

    Note maxillary hypoplasia, ocular proptosis with mild relative prognathism. (From Renier et al. 2000) syndrome is genetically heterogeneous.[rrnursingschool.biz] Crouzon craniofacial dysostosis (OMIM 123500) involves only the face and skull.[rrnursingschool.biz] The distinguishing dysmorphism consists in underdevelopment of the midfacial bones, resulting in shallow orbits with ex-ophthalmos, and prognathism with inverted dental occlusion[rrnursingschool.biz]

  • Baller-Gerold Syndrome

    Note maxillary hypoplasia, ocular proptosis with mild relative prognathism. (From Renier et al. 2000) syndrome is genetically heterogeneous.[rrnursingschool.biz] Crouzon craniofacial dysostosis (OMIM 123500) involves only the face and skull.[rrnursingschool.biz] The distinguishing dysmorphism consists in underdevelopment of the midfacial bones, resulting in shallow orbits with ex-ophthalmos, and prognathism with inverted dental occlusion[rrnursingschool.biz]

  • Robinow-Sorauf Syndrome

    The leptoprosopic flat face with mild maxillary hypoplasia and relative mandibular prognathism was exemplified by a prominent chin [Figure 2] .[ijdentistry.com] Clin Dysmorph 2:189–198 PubMed CrossRef Google Scholar Robinow M (1995) Living history — autobiography: pediatric genetics in a New World.[link.springer.com] maxillary hypoplasia and relativemandibular prognathism exemplified by a prominent.Wide root of the nose, thick eyebrows, prominenteyelashes, mild convergent strabismus and[docslide.com.br]

  • 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] (craniofacial dysmorphism), breathing and feeding difficulties (dysphagia), and urogenital abnormalities.[rarediseases.org] Dysmorphic features: high anterior hairline, long face with prognathism, long nose, broad nasal bridge with underdeveloped alae nasi, asymmetic ears, narrow mouth.[gene.sfari.org]

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