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12 Possible Causes for Mild Maxillary Prognathism, Tall Stature

  • Chromosome 22q13.3 Deletion Syndrome
  • Craniosynostosis Type 3

    Note maxillary hypoplasia, ocular proptosis with mild relative prognathism. (From Renier et al. 2000) syndrome is genetically heterogeneous.[rrnursingschool.biz] Dravidians tend to be of relatively tall stature. Their skin ranges from brown to almost black. Eyes are dark brown or black.[internetlooks.com] Whites tend to be of relatively tall stature. They have white or tan skin. The tan on some can be quite dark. The eyes are black, brown, blue, green, hazel or grey.[internetlooks.com]

  • Familial Scaphocephaly Syndrome

    Note maxillary hypoplasia, ocular proptosis with mild relative prognathism. (From Renier et al. 2000) syndrome is genetically heterogeneous.[rrnursingschool.biz] Of 19 unaffected individuals, three had macrocephaly with tall stature, and none had scaphocephaly.[jmg.bmj.com]

  • Isolated Trigonocephaly

    Note maxillary hypoplasia, ocular proptosis with mild relative prognathism. (From Renier et al. 2000) syndrome is genetically heterogeneous.[rrnursingschool.biz] stature and mental retardation, Clinical Dysmorphology, 10.1097/MCD.0b013e32833c8ba1, 19, 4, (190-194), (2010).[doi.org] Gillessen-Kaesbach, A de novo unbalanced translocation leading to partial monosomy 9p23-pter and partial trisomy 15q25.3-qter associated with 46,XY complete gonadal dysgenesis, tall[doi.org]

  • 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] CADASIL NGS panel HTRA1, NOTCH3 Del Dup NGS Caffey disease COL1A1 Del Dup NGS Campomelic dysplasia SOX9 Del Dup NGS Camptodactyly, tall stature, and hearing loss syndrome[ctgt.net] People with a syndrome can also be mentally challenged, have developmental delay and are born with tall stature.[nipt.ng]

  • Baller-Gerold Syndrome

    Note maxillary hypoplasia, ocular proptosis with mild relative prognathism. (From Renier et al. 2000) syndrome is genetically heterogeneous.[rrnursingschool.biz] Karger AG, Basel References Baron J, Savendahl L, De Luca F, Dauber A, Phillip M, Wit JM, et al: Short and tall stature: a new paradigm emerges.[karger.com] Makrythanasis P, Temtamy S, Aglan MS, Otaify GA, Hamamy H, Antonarakis SE: A novel homozygous mutation in FGFR3 causes tall stature, severe lateral tibial deviation, scoliosis[karger.com]

  • Micrognathism

    […] of the teeth -Mild prognathism www.indiandentalacademy.com 19.  Hypoparathyroidism - retarded eruption -early exfoliation -enamel defects  Hyperparathyroidism - demineralization[slideshare.net] The proband had some marfanoid manifestations: arachnodactyly, tall stature, and 'skinniness.' Fragile skin, loose joints and cigarette-paper scars were present.[findzebra.com] .  Hypothyroidism - Growth retardation - Delayed eruption of the teeth - Maxillary protrusion - Spacing  Hyperthyroidism - Accelerated skeletal growth - Irregular eruption[slideshare.net]

  • Mandibuloacral Dysostosis

    […] with mild maxillary hypoplasia [Figure 8] .[jiaomr.in] Multiple exostoses Skeletal muscle hypertrophy Hypoplasia of the radius Short toe Tall stature High, narrow palate Pica Madelung deformity Mesomelic short stature Thickened[mendelian.co] Occasional findings include a metabolic abnormalities, thyroid hemiagenesis, collagenoma, diabetes mellitus, and marfanoid habitus (tall stature with long and thin limbs,[medcraveonline.com]

  • De Hauwere Syndrome

    Nonocular features included characteristic facies (maxillary hypoplasia, short philtrum, and protruding lower lip of mild prognathism), dental anomalies (microdontia, hypodontia[genome.jp] […] hydrocephalus (onset in infancy), tall stature, joint laxity, and thoracolumbar kyphosis.[findzebra.com] stature-scoliosis-hearing loss syndrome CANOMAD Syndrome Cantalamessa Baldini Ambrosi Syndrome Cantu Sanchez-Corona Fragoso Syndrome Capgras syndrome capillary leak syndrome[rgd.mcw.edu]

  • 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] stature Encephalocele Occipital encephalocele Retinal coloboma Molar tooth sign on MRI Cephalocele Tented upper lip vermilion Dandy-Walker malformation Open mouth Absent[mendelian.co] maxillary hypoplasia and relative mandibular prognathism exemplifi ed by a prominent, wide root of the nose, thick eyebrows, prominent eyelashes, mild convergent strabismus[ijdentistry.com]

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