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27 Possible Causes for Buccal Frenulae, Failure to Thrive, Hearing Impairment

  • Growth Delay-Hydrocephaly-Lung Hypoplasia Syndrome

    Related symptoms: Global developmental delay Hearing impairment Scoliosis Muscular hypotonia High palate SOURCES: ORPHANET More info about FRIED SYNDROME Medium match PROLIFERATIVE[mendelian.co] […] to thrive, short stature, feeding difficulties, sternal deformity, renal malformation, pubertal delay, cryptorchidism, developmental or behavioral problems, vision problems[aafp.org] 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]

  • X-Linked Mandibulofacial Dysostosis

    Showing of 29 80%-99% of people have these symptoms Branchial anomaly 0009794 Conductive hearing impairment Conductive deafness Conductive hearing loss [ more ] 0000405 Downslanted[rarediseases.info.nih.gov] […] to thrive, Growth retardation, Congenital malformations (30%-50%) 1:100,000 and 1:200,000 Age of onset: 1 year Dyserythropoietic anemia COX4I2, C15orf41, KIF23, KLF1 Moderate[centogene.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]

  • Saethre-Chotzen Syndrome

    Complete Probemix List New and Improved Products IVD-Registered Products Bacteria Blood Cancers Cardiovascular Carrier Endocrine & Reproductive Gastrointestinal & Liver Hearing[mlpa.com] frenula, limb defects, visceral anomalies involving the genitalia, heart, and intestine, redundant skin, joint contractures and dislocations, hemangiomas, mental deficiency[rrnursingschool.biz] In addition, mild hearing impairment is frequent.[rarediseases.org]

  • Growth Failure

    […] gene s ; decreased formation of hydrogen and disulfide bonds between type 1 preprocollagen molecules decreased triple helix formation defective type I collagen synthesis impaired[amboss.com] Presentation on theme: "Faltering growth(failure to thrive)"— Presentation transcript: 1 Faltering growth(failure to thrive) refers to not only failure of growth(suboptimal[slideplayer.com] Variable features include laryngeal cleft, abnormal lung lobulation, renal agenesis and/or renal dysplasia, short 4th metacarpals, nail dysplasia, multiple buccal frenula,[analesdepediatria.org]

  • Smith Lemli Opitz Syndrome

    It is characterized by growth and developmental delay, vision and hearing impairment, and impairment of the peripheral nervous system function.[icd10data.com] Affected individuals have dysmorphism, short stature, failure to thrive, microcephaly, multiple congenital malformations, and mental retardation.[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]

  • Hypotonia-Failure to Thrive-Microcephaly Syndrome

    impairment DIGEORGE SYNDROME( VELO CARDIO-FACIAL) SYNDROME Hypoplasia or agenesis of the thymus Hypoplasia/ Agenesis of parathyroid glands Hypoplasia of auricle and external[paediatricks.com] […] rare fatal neurometabolic developmental disorder characterized clinically by muscular hypotonia, psychomotor retardation, failure to thrive, and microcephaly.[orpha.net] 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]

  • Pallister-Hall Syndrome

    impairment Underdeveloped or improperly developed genitals Gastrointestinal defects, abnormal kidney function Reduced growth of head size and body length Severe mental retardation[dovemed.com] […] to thrive cyanosis regurgitation/reflux DIFFERENTIAL DIAGNOSIS laryngomalacia vocal cord paralysis laryngopharyngeal reflux disease neuromuscular swallowing disorder reactive[laryngeal-cleft.com] frenula microglossia cleft lip and palate teeth natal teeth cardiovascular anomalies ventricular septal defect patent ductus arteriosus proximal aortic coarctation respiratory[humpath.com]

  • Baller-Gerold Syndrome

    impairment Conductive deafness Conductive hearing loss [ more ] 0000405 Epicanthus Eye folds Prominent eye folds [ more ] 0000286 Hydronephrosis 0000126 Hypertelorism Wide-set[rarediseases.info.nih.gov] frenula, limb defects, visceral anomalies involving the genitalia, heart, and intestine, redundant skin, joint contractures and dislocations, hemangiomas, mental deficiency[rrnursingschool.biz] impairment, corneal clouding, dental abnormalities, and hepatomegaly 1, 5 .[centogene.com]

  • Autosomal Dominant Mandibulofacial Dysostosis with Ptosis

    Stickler syndrome Hearing impairment Treacher Collins-Franceschetti syndrome Hearing impairment Usher syndrome Hearing impairment Waardenburg syndrome Hearing impairment[genomediagnosticsnijmegen.nl] However, he was hospitalized immediately after birth for failure to thrive. Rest of the neonatal course and infancy were unremarkable.[jofs.in] 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]

  • Familial Median Cleft of the Upper and Lower Lips

    impairment or loss Intellectual disability (rare) Central Nervous System abnormalities What are the treatment options?[houstoncraniofacial.com] The goal is to provide adequate nutrition to satisfy the caloric requirements and avoid failure to thrive.[pocketdentistry.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]

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