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29 Possible Causes for Brachycephaly, Buccal Frenulae, Cleft Palate

  • Saethre-Chotzen Syndrome

    In our patients, high-arched palate was noted in 43%, bifid uvula in 10%, and cleft palate in 6%.[ncbi.nlm.nih.gov] frenula, limb defects, visceral anomalies involving the genitalia, heart, and intestine, redundant skin, joint contractures and dislocations, hemangiomas, mental deficiency[rrnursingschool.biz] […] persons in five generations are affected with a complex of skeletal malformations which variably includes peculiar asymmetric facies, delayed closure of large fontanels, brachycephaly[ncbi.nlm.nih.gov]

  • Familial Scaphocephaly Syndrome

    Summary Although syndromic cleft lip and palate is occasionally associated with other anomalies, even with craniosynostosis, non-syndromic cleft lip and palate is rarely seen[link.springer.com] frenula, limb defects, visceral anomalies involving the genitalia, heart, and intestine, redundant skin, joint contractures and dislocations, hemangiomas, mental deficiency[rrnursingschool.biz] Brachycephaly Brachycephaly is flattening of the back of the skull, caused by the baby lying on its back for too long.[moveforwardpt.com]

  • Isolated Brachycephaly

    […] lip/cleft palate and other lip and palatal anomalies, bifid uvula, choanal atresia, macrotia with lateral facial cleft, craniosynostosis, frontal bossing, frontal encephalocele[bredagenetics.com] frenula, limb defects, visceral anomalies involving the genitalia, heart, and intestine, redundant skin, joint contractures and dislocations, hemangiomas, mental deficiency[rrnursingschool.biz] We did not observe any significant alteration of FM in patients with isolated brachycephaly compared to control group.[ncbi.nlm.nih.gov]

  • Isolated Trigonocephaly

    Cleft palate without cleft lip is a distinct disorder.[sonoworld.com] 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] Brachycephaly in a 6-month-old baby girl with bi- seen, as is retrusion of the supraorbital rim, root of the nose, lateral coronal synostosis.[rrnursingschool.biz]

  • X-Linked Mandibulofacial Dysostosis

    Section on children from conception to age three covers conditions such as cleft palate, disturbances in calcification, unusual numbers of teeth, oral habits, caries, and[books.google.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,[widesmiles2.org] ; Brachycephaly; scaphocephaly; trigonocephaly; “cloverleaf” skull (kleeblattschädel) scaphocephaly; trigonocephaly; cloverleaf” (kleeblattschädel) Ocular proptosis: blindness[slideshare.net]

  • Simpson Dysmorphia Syndrome

    […] and cleft palate.[oatext.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,[widesmiles2.org] ) 759.89 Disease, diseased - see also Syndrome Bruck-de Lange (Amsterdam dwarf, intellectual disabilities, and brachycephaly) 759.89 Cockayne's (microcephaly and dwarfism)[icd9data.com]

  • Pallister W Syndrome

    The features of Pallisker killian rarely involved cleft palate and anorectal anomalies (2).[latunisiemedicale.com] 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] ) 759.89 Disease, diseased - see also Syndrome Bruck-de Lange (Amsterdam dwarf, intellectual disabilities, and brachycephaly) 759.89 Cockayne's (microcephaly and dwarfism)[icd9data.com]

  • Autosomal Dominant Prognathism

    , cleft palate, malformed ears TF Paired box homeotic gene-3 PAX3 2q35 193500 Waardenburg syndrome, type I 193500 AD wide nasal bridge, short philtrum, cleft lip or palate[en.wikibooks.org] Patients have a distinctive facial appearance which includes low-set ears, brachycephaly, hypertelorism, exophthalmos, and mandibular prognathism.[icd10data.com] CCD is characterized by brachycephaly, hypertelorism, prominent orbital ridges, the inferior margin reduced to the small maxillae, and relative mandibular prognathism [ 1[e-acfs.org]

  • Gorlin Psaume Syndrome

    Cleft palate and lobed, bifid tongue.ognized (Table 1).[docslide.us] frenulae, bilateral preaxial polydactyly of feet and postaxial polydactyly of hands) accompanied by microcephaly, micropenis and severe intellectual disabilities.[ciliajournal.biomedcentral.com] ) 759.89 Disease, diseased - see also Syndrome Bruck-de Lange (Amsterdam dwarf, intellectual disabilities, and brachycephaly) 759.89 Cockayne's (microcephaly and dwarfism)[icd9data.com]

  • Baller-Gerold Syndrome

    Mouth and oral structures: Cleft palate, bifid uvula, and highly arched palate. Hand and foot: Aplastic or hypoplastic thumbs.[whonamedit.com] frenula, limb defects, visceral anomalies involving the genitalia, heart, and intestine, redundant skin, joint contractures and dislocations, hemangiomas, mental deficiency[rrnursingschool.biz] Clinical description Craniosynostosis and radial ray anomalies present at birth and are associated with facial dysmorphism (brachycephaly, ocular exophthalmia, frontal bossing[orpha.net]

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