Create issue ticket

869 Possible Causes for Maxillary Hypoplasia

  • Ringed Hair Disease

    Maxillary hypoplasia was significant in many patients, the brittle, short hair, reduced eyelashes, crowded teeth, and dull appearance created a characteristic facial appearance[]

  • Cerebro-Facio-Thoracic Dysplasia

    […] retardation, characteristic facies, narrow forehead, bushy eyebrows with synophrys, hypertelorism, broad nose, wide philtrum, triangular-shaped mouth, short neck, marked maxillary[] X-ray of the skull showed brachycephaly, with marked hypoplasia of the superior niaxillary bones and poorly-developed frontal and maxillary sinuses.[] hypoplasia, a low hairline (especially posteriorly in the midline on the neck), brachycephaly, calcified clinoid ligaments, and multiple bony abnormalities in the upper thoracic[]

  • Leukoencephalopathy - Metaphyseal Chondrodysplasia Syndrome

    Hypoplasia and Brachydactyly Metaphyseal Dysplasia with Maxillary Hypoplasia with or without Brachydactyly Metaphyseal Dysplasia without Hypotrichosis Metaphyseal Dysplasia[] hypoplasia with or without brachydactyly Gene Set From OMIM Gene-Disease Associations genes associated with the metaphyseal dysplasia with maxillary hypoplasia with or without[] […] and distinctive facial appearance Mental retardation X-linked, South African type Mental retardation, anterior maxillary protrusion, and strabismus Mental retardation, autosomal[]

  • Kleiner Holmes Syndrome

    […] fossa arachnoid cyst; Hydrocephalus]; #101400:Saethre-Chotzen syndrome [Short stature; Brachycephaly; Acrocephaly; Flat face; High, flat forehead; Low frontal hairline; Maxillary[] […] second and third toes; Short, broad metatarsal; Tarsonavicular and calcaneonavicular fusion]; #123500:Crouzon syndrome [Craniosynostosis; Brachycephaly; Frontal bossing; Maxillary[] […] femoral fractures; Ulnar bowing; Joint contractures; Arachnodactyly; Camptodactyly; Rocker-bottom feet; Variable mental retardation; Hydrocephalus]; #609579:Scaphocephaly, maxillary[]

  • X-Linked Dominant Chondrodysplasia Type Chassaing-Lacombe

    hypoplasia - brachydacty Microphthalmia, Lenz type Oculofaciocardiodental syndrome Congenital bilateral absence of vas deferens Cystic fibrosis Hereditary chronic pancreatitis[] hypoplasia-brachydacty syndrome Metatropic dysplasia Microbrachycephaly-ptosis-cleft lip syndrome Microcephalic osteodysplastic dysplasia, Saul-Wilson type Microcephalic[] […] glioblastoma Gliosarcoma Familial cylindromatosis Familial multiple trichoepithelioma Lissencephaly due to TUBA1A mutation Cleidocranial dysplasia Metaphyseal dysplasia - maxillary[]

  • Axenfeld-Rieger Syndrome Type 3

    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.[] Systemic anomalies include craniofacial dysmorophisms such as hypertelorism, telecanthus, maxillary hypoplasia, and a broad, flat nasal bridge.[] Anomalies include anterior segment dysgenesis of the eye, dental anomalies, maxillary hypoplasia, periumbilical anomalies, and congenital heart defects.[]

  • Humero-Radial Synostosis

    hypoplasia, proptosis, high palate, arachnodacyly, pectus excavatum, hernias, fusion of C1 & C2 vertebrae Loeys-Deitz Syndrome: Traits Craniosynostosis, ID, congenital heart[] […] eyes Opitz C Syndrome: Skeletal Features Polydactyly, anomalous ribs, short limbs, transverse limb reductions Shpintxen-Goldberg Syndrome: Traits Craniosynostosis, DD, ID, Maxillary[]

  • Brachydactylous Dwarfism Type Mseleni

    […] dysplasia—maxillary hypoplasia—brachydacty metaphyseal dysplasia with maxillary hypoplasia and brachydactyly 293830 Constitutional dyserythropoietic anemia congenital dyserythropoietic[] Diseases Teeth noneruption of with maxillary hypoplasia and genu valgum Trisomy 6 Kleeblattschaedel syndrome Bixler Christian Gorlin syndrome Papilledema Familial multiple[] […] thumbs—hypospadias—maxillary diastema radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema 156731 Dyssegmental dysplasia, Rolland-Desbuquois type dyssegmental[]

  • Glucose-6-Phosphate Dehydrogenase Deficiency

    Maxillary hypoplasia, deep palatal vault, anterior open bite, crowding of the dental arch, severely delayed tooth eruption, and dental malocclusion are the main oral manifestations[] Apert syndrome is characterized by midface hypoplasia, syndactyly of the hands and feet, proptosis of eyes, steep and flat frontal bones, and premature union of cranial sutures[]

  • Hairy Leukoplakia

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

Further symptoms

Similar symptoms