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27 Possible Causes for Buccal Frenulae, Craniosynostosis, Failure to Thrive

  • Growth Delay-Hydrocephaly-Lung Hypoplasia Syndrome

    […] and dental anomalies IL11RA Craniosynostosis type 1 TWIST1 Craniosynostosis type 2 MSX2 Craniosynostosis type 3 TCF12 Craniosynostosis type 4 ERF Craniosynostosis type 6[centogene.com] […] 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]

  • Pallister-Hall Syndrome

    Craniosynostosis was noted in several of the earliest GCPS case reports, but we have observed this in very few patients.[ojrd.biomedcentral.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

    Baller-Gerold syndrome (BGS) is a rare autosomal recessive condition with radial aplasia/hypoplasia and craniosynostosis (OMIM 218600).[ncbi.nlm.nih.gov] […] of the radius 0006501 Aplasia/Hypoplasia of the thumb Absent/small thumb Absent/underdeveloped thumb [ more ] 0009601 Brachyturricephaly High, prominent forehead 0000244 Failure[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]

  • X-Linked Mandibulofacial Dysostosis

    Apert syndrome 101200 AD craniosynostosis, brachysphenocephalic acrocephaly, flat facies, high narrow palate Pfeiffer syndrome 101600 AD mild craniosynostosis, flat facies[widesmiles2.org] […] 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] However, he was hospitalized immediately after birth for failure to thrive. Rest of the neonatal course and infancy were unremarkable.[jofs.in]

  • Saethre-Chotzen Syndrome

    Furthermore, craniosynostosis was not present at birth or at the age of 4 months.[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] Craniosynostosis can happen before the baby is born or during the first few months of life.[sickkids.ca]

  • Autosomal Dominant Prognathism

    Association with mildly everted lower eyelids, flat malar area, thickened lower lip and craniosynostosis has been reported.[orpha.net] […] to thrive SOURCES: OMIM NCIT SCTID ORPHANET More info about MELANOCYTIC NEVUS SYNDROME, CONGENITAL; CMNS Low match DIAMOND-BLACKFAN ANEMIA 6; DBA6 Diamond-Blackfan anemia[mendelian.co] 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]

  • Hypotonia-Failure to Thrive-Microcephaly Syndrome

    Agenesis of the corpus callosum, Atrial Septal Defect, micrognathia, broad thumbs, microcephaly, Failure to thrive, developmental delay, very small stature, and craniosynostosis[myresults.org] […] 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]

  • Familial Scaphocephaly Syndrome

    Craniosynostosis Causes Craniosynostosis is usually an isolated finding in an otherwise normal child. The precise causes vary and are incompletely understood.[chla.org] Failure to thrive can occur in the absence of nutritional support (e.g., nasogastric tube, feeding gastrostomy).[pocketdentistry.com] frenula, limb defects, visceral anomalies involving the genitalia, heart, and intestine, redundant skin, joint contractures and dislocations, hemangiomas, mental deficiency[rrnursingschool.biz]

  • Smith Lemli Opitz Syndrome

    2 Craniosynostosis Mental Retardation Clefting Syndrome Craniosynostosis-Mental Retardation Syndrome of Lin and Gettig Cree Mental Retardation Syndrome crescentic glomerulonephritis[rgd.mcw.edu] 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]

  • Craniosynostosis with Ocular Abnormalities and Hallucal Defects

    Craniosynostosis syndrome MedGen UID: 1163 • Concept ID: C0010278 • Disease or Syndrome A congenital disorder characterized by earlier than normal closure of some or all sutures[ncbi.nlm.nih.gov] Related symptoms: Intellectual disability Generalized hypotonia Failure to thrive Delayed speech and language development Macrocephaly SOURCES: OMIM UMLS GARD MONDO More info[mendelian.co] […] between the buccal mucous membrane and alveolar ridge.[plasticsurgerykey.com]

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