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36 Possible Causes for Buccal Frenulae, Congenital Abnormality

  • Smith Lemli Opitz Syndrome

    Abstract Patients with Smith-Lemli-Opitz syndrome (SLOS) are born with multiple congenital abnormalities.[ncbi.nlm.nih.gov] 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.[ajnr.org] It is manifested with multiple congenital malformations, including facial abnormalities, microcephaly, and syndactyly. Behavioral abnormalities may also be present.[icd10data.com]

  • Baller-Gerold Syndrome

    frenula, limb defects, visceral anomalies involving the genitalia, heart, and intestine, redundant skin, joint contractures and dislocations, hemangiomas, mental deficiency[rrnursingschool.biz] Additional congenital abnormalities included midface hypoplasia, atrial and ventricular septal defects, right hydronephrosis, partial sacral agenesis, and anterior ectopic[ncbi.nlm.nih.gov] Code Classification Congenital malformations, deformations and chromosomal abnormalities ( Q00-Q99 ) Congenital malformations and deformations of the musculoskeletal system[icdlist.com]

  • Simpson Dysmorphia Syndrome

    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,[widesmiles2.org] , distinctive craniofacial features, macrocephaly, variable congenital malformations, organomegaly, increased risk of tumor and mild/moderate intellectual deficiency.[hal.archives-ouvertes.fr] frenula -microglossia -micrognathia -cleft palate -malformed ears describe waardenburg syndrome type I -autosomal dominant -wide nasal bridge -short philtrum -cleft lip or[brainscape.com]

  • Pallister-Hall Syndrome

    Pallister-Hall syndrome is a rare, autosomal dominant, genetic disorder characterized by different congenital abnormalities: hypothalamic hamartoblastoma, bifid or shortened[ncbi.nlm.nih.gov] frenula microglossia cleft lip and palate teeth natal teeth cardiovascular anomalies ventricular septal defect patent ductus arteriosus proximal aortic coarctation respiratory[humpath.com] malformations) and present in a very different and stereotypical fashion with gelastic seizures and/or precocious puberty.[ncbi.nlm.nih.gov]

  • Familial Median Cleft of the Upper and Lower Lips

    CONSUMERS: Click here for the Consumer Version Congenital craniofacial abnormalities are a group of defects caused by abnormal growth and/or development of the head and facial[merckmanuals.com] 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,[en.wikibooks.org] Examination revealed no other congenital abnormalities. There was no significant family history. The pit was treated successfully with excision.[casereports.bmj.com]

  • Growth Failure

    TABLE 1 Characteristics of 362 833 Infants Weighing 501 to 1500 g Without Congenital Malformations Who Were Inborn at Vermont Oxford Network North American Member Centers,[pediatrics.aappublications.org] Variable features include laryngeal cleft, abnormal lung lobulation, renal agenesis and/or renal dysplasia, short 4th metacarpals, nail dysplasia, multiple buccal frenula,[analesdepediatria.org] , cardiac defects (congenital heart disease, cardiac arrhythmia, heart abnormalities, hypertrophic cardiomyopathy) and cutaneous anomalies and increased risk of tumors such[amhsr.org]

  • X-Linked Mandibulofacial Dysostosis

    (attribute)' and the value is a subtype of 'Congenital dysplasia (morphologic abnormality)' .[vtsl.vetmed.vt.edu] 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,[widesmiles2.org] abnormality syndrome that is characterized by microcephaly, malar hypoplasia with downslanting palpebral fissures, highly arched palate, apparently low-set and protruding[malacards.org]

  • Gorlin Psaume Syndrome

    ICD-10-CM Codes › Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities › Q80-Q89 Other congenital malformations › Q87- Other specified congenital malformation[icd10data.com] frenulae, bilateral preaxial polydactyly of feet and postaxial polydactyly of hands) accompanied by microcephaly, micropenis and severe intellectual disabilities.[ciliajournal.biomedcentral.com] These fibrous bands are hyperplastic frenulae extending from the buccal mucous membrane to the alveolar ridge, resulting in notching of the alveolar ridges.[pocketdentistry.com]

  • Isolated Trigonocephaly

    It was first reported by Opitz, et al. in 1969 and is characterized by trigonocephaly (prominent metopic sutures), multiple buccal frenula, polydactyly, skin laxity, primordial[indianpediatrics.net] Congenital microphthalmia is frequently associated with visual disorders and with other anomalies.[sonoworld.com] frenula, limb defects, visceral anomalies involving the genitalia, heart, and intestine, redundant skin, joint contractures and dislocations, hemangiomas, mental deficiency[rrnursingschool.biz]

  • Growth Delay-Hydrocephaly-Lung Hypoplasia Syndrome

    WHO-ICD-10 version:2010 Congenital malformations, deformations and chromosomal abnormalities Congenital malformations of the nervous system Mode of Inheritance Autosomal recessive[cags.org.ae] frenulae (skin connecting the cheek to the gums) Depressed nasal bridge Anterverted nares (nasal openings are tipped upwards) Low-set posteriorly rotated ears Retrognathia[bohring-opitz.org] Nervous-system disorders Congenital malformations of the nervous system rank among the most common severe congenital abnormalities.[britannica.com]

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