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236 Possible Causes for Anteverted Nostril, Buccal Frenulae, High, Flat Forehead

  • Pallister-Hall Syndrome

    The high school will also begin a new daily schedule that follows a 6-day cycle and rotates classes each day.[] […] developmental delays Hearing loss, lack of speech development Issues related to the face and skull: Sparse scalp hair, eyebrows and eyelashes Coarse facial features Large forehead[] frenula microglossia cleft lip and palate teeth natal teeth cardiovascular anomalies ventricular septal defect patent ductus arteriosus proximal aortic coarctation respiratory[] (anteverted nares) and a broad or flat nasal bridge; and/or an unusually long vertical groove in the middle of the upper lip (philtrum).[]

  • Smith Lemli Opitz Syndrome

    […] by natural antioxidant defense mechanisms including the high-density lipoprotein (HDL)-associated paraoxonase-1 (PON1) enzyme.[] A characteristic craniofacial pattern profile was universally present: narrow forehead, brachycephaly, short palpebral fissures, short nasal ridge, anteverted nares, flat[] Facial anomalies, which include wide and flat nasal bridge, small sized nose with an upturned tip or pug nose, anteverted nostrils, undersized jaw (micrognathia), the ear[] These include a short nose with flat nasal bridge, low-set and posteriorly angulated ears, cleft palate, cleft uvula, buccal frenula, bifid epiglottis, and cleft larynx.[]

  • Pallister-Killian Syndrome

    The prevalence of oral habits (non-nutritive sucking, mouth breathing, bruxism) was high, even in older probands.[] Craniofacial manifestations include a coarse'' face with flat profile, high forehead with temporo-frontal balding, sparseness of eyebrows and lashes, shallow supraorbital[] Table 2 Clinical features 1 Female 18y/22y Flat, broad nasal root, upslanting palpebral fissures, hypertelorism, coarse face, anteverted nostrils, retrognathia, small ears[] The dysmorphic features included a board forehead with high anterior hairline, hypertelorism, flat nasal bridge, short upturned nose, down turned corners of the mouth, short[]

    Missing: Buccal Frenulae
  • Saethre-Chotzen Syndrome

    However, they did distinguish themselves by the presence of many additional anomalies and diseases and--most importantly--the high frequency of mental retardation, which was[] Saethre-Chotzen Syndrome Characteristics Most parents notice the child has a lopsided or tall, flat forehead.[] nostrils, thin upper lip, long philtrum, high palate, micrognathia, short neck, enlarged internipple distance, tapering fngers, flat feet, and hypotonia.[] frenula, limb defects, visceral anomalies involving the genitalia, heart, and intestine, redundant skin, joint contractures and dislocations, hemangiomas, mental deficiency[]

  • Autosomal Dominant Mandibulofacial Dysostosis with Ptosis

    High resolution karyotype was normal.[] Examination At 3 yr (Fig 2b) she was an alert girl with curly brown hair, a flat and high forehead with a horizontal groove above the eyebrows, telecanthus (inner canthal[] Dolichocephaly, right anterior upsweep of hairline, small nose with flat root, hypoplastic tip and small anteverted nostrils with mouth-breathing facial changes (Fig. la);[] frenula, microglossia, micrognathia, cleft palate, malformed ears TF Paired box homeotic gene-3 PAX3 2q35 193500 Waardenburg syndrome, type I 193500 AD wide nasal bridge,[]

  • X-Linked Mandibulofacial Dysostosis

    […] hearing impairment Conductive deafness Conductive hearing loss [ more ] 0000405 Downslanted palpebral fissures Downward slanting of the opening between the eyelids 0000494 High[] , dolichoturricephaly, large fontanels, flat face, round face, hypoplastic supraorbital ridge, epicanthus, cleft palate TM Diastrophic dysplasia sulfate transporter DTDST[] The nasal bridge is low and the nostrils anteverted. The zygomatic arches may be absent. The nipples are often missing as well.[] Affiliated tissues include bone, and related phenotypes are high palate and microcephaly[]

  • Growth Delay-Hydrocephaly-Lung Hypoplasia Syndrome

    […] der(17)(D17S379-, RARA ) Miller-Dieker Lissencephaly Syndrome (MDLS; 17p13.3): typical facies (bitemporal hollowing, thin downturned upper lip, micrograthia; micocephaly, high[] The face has been described as dysmorphic with a high forehead, flat nasal bridge, a cloverleaf-shaped skull, and hypoplastic cranial bones with premature suture closure.[] frenulae (skin connecting the cheek to the gums) Depressed nasal bridge Anterverted nares (nasal openings are tipped upwards) Low-set posteriorly rotated ears Retrognathia[] Read more about the high-risk prenatal care services at the Fetal Medicine Institute of Children’s National.[]

  • Mucopolysaccharidosis 1H

    However, large studies have shown that preparative regimen-related toxicity (RRT) and graft failure rates have been relatively high.[] The facial features undergo a marked deterioration, which mainly include a low nasal bridge, flat face, and protruding forehead.[] nostrils, full cheeks and enlarged lips), cardiomyopathy and valvular abnormalities, neurosensorial hearing loss, enlarged tonsils and adenoids, and nasal secretion.[] Distinct facial features (including flat face, depressed nasal bridge, and bulging forehead) become more evident in the second year.[]

    Missing: Buccal Frenulae
  • Pallister W Syndrome

    High cholesterol and high blood pressure can contribute to the buildup of plaques in your arteries.[] The facial features include prominent mandible, pugilistic appearance, orofacial cleft, broad flat nasal bridge and jaw, partial adontia, high broad forehead, broad uvula,[] These include a short nose with flat nasal bridge, low-set and posteriorly angulated ears, cleft palate, cleft uvula, buccal frenula, bifid epiglottis, and cleft larynx.[] nostrils small and apparently low-set ears simian crease clinodactyly congenital heart disease : may be seen in up to 25% of cases 4 congenital diaphragmatic hernia : may[]

  • Zellweger Syndrome

    The accuracy, high-throughput and speed of the method make it suitable for clinical application.[] On physical examination, the child had flat facies, flat occiput, high forehead, upward slanting of palpebral fissures, hypertelorism, epicanthal folds and anteverted nares[] ) nostrils vertical fold of skin over the inner corner of the eye (epicanthal fold) upslanting eyes shallow orbital ridges minor ear abnormalities Other characteristics include[] Symptoms of the Zellweger spectrum of disease include: High forehead Flat occiput: The occiput is the bone forming the back of the skull, and encloses the hole where the spinal[]

    Missing: Buccal Frenulae

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