Create issue ticket

2,022 Possible Causes for Craniosynostosis, Multiple Buccal Frenula, Syndactyly between Adjacent Toes

  • Pallister-Hall Syndrome

    ) Syndactyly (abnormal "webbing" between, or fusing of, adjacent fingers and/or toes) Short limbs Dysplastic nails ( i.e., finger nails and toe nails that are flaky and poorly[brighthub.com] buccal frenula microglossia cleft lip and palate teeth natal teeth cardiovascular anomalies ventricular septal defect patent ductus arteriosus proximal aortic coarctation[humpath.com] Craniosynostosis was noted in several of the earliest GCPS case reports, but we have observed this in very few patients.[ojrd.biomedcentral.com]

  • Craniosynostosis Type 3

    buccal frenula, limb defects, visceral anomalies involving the genitalia, heart, and intestine, redundant skin, joint contractures and dislocations, hemangiomas, mental deficiency[rrnursingschool.biz] Etiology of Craniosynostosis The etiology of nonsyndromic craniosynostosis is unknown, and the condition is sporadic in most instances.[aafp.org] "Types of Craniosynostosis". Craniosynostosis Surgery in South Texas. "What is Craniosynostosis?".[en.wikipedia.org]

  • 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] Common Syndromic Craniosynostosis like Apert and Crouzon have prevalence of about 1 in 65000, each about 4-6 per cent of all craniosynostosis.[childneurosurgeon.com] buccal frenula, limb defects, visceral anomalies involving the genitalia, heart, and intestine, redundant skin, joint contractures and dislocations, hemangiomas, mental deficiency[rrnursingschool.biz]

    Missing: Syndactyly between Adjacent Toes
  • Saethre-Chotzen Syndrome

    buccal frenula, limb defects, visceral anomalies involving the genitalia, heart, and intestine, redundant skin, joint contractures and dislocations, hemangiomas, mental deficiency[rrnursingschool.biz] Furthermore, craniosynostosis was not present at birth or at the age of 4 months.[ncbi.nlm.nih.gov] Craniosynostosis can happen before the baby is born or during the first few months of life.[sickkids.ca]

    Missing: Syndactyly between Adjacent Toes
  • Familial Scaphocephaly Syndrome

    buccal frenula, limb defects, visceral anomalies involving the genitalia, heart, and intestine, redundant skin, joint contractures and dislocations, hemangiomas, mental deficiency[rrnursingschool.biz] Craniosynostosis Causes Craniosynostosis is usually an isolated finding in an otherwise normal child. The precise causes vary and are incompletely understood.[chla.org] However, most children with craniosynostosis are otherwise healthy and have normal intelligence. Symptoms & Types Symptoms depend on the type of craniosynostosis.[texaschildrens.org]

    Missing: Syndactyly between Adjacent Toes
  • Baller-Gerold Syndrome

    buccal frenula, limb defects, visceral anomalies involving the genitalia, heart, and intestine, redundant skin, joint contractures and dislocations, hemangiomas, mental deficiency[rrnursingschool.biz] Baller-Gerold syndrome (BGS) is a rare autosomal recessive condition with radial aplasia/hypoplasia and craniosynostosis (OMIM 218600).[ncbi.nlm.nih.gov] The cardinal features of the Baller-Gerold syndrome (MIM *21860) are craniosynostosis and radial aplasia.[ncbi.nlm.nih.gov]

    Missing: Syndactyly between Adjacent Toes
  • Autosomal Dominant Prognathism

    buccal frenula, microglossia, micrognathia, cleft palate, malformed ears TF Paired box homeotic gene-3 PAX3 2q35 193500 Waardenburg syndrome, type I 193500 AD wide nasal[en.wikibooks.org] Association with mildly everted lower eyelids, flat malar area, thickened lower lip and craniosynostosis has been reported.[orpha.net] Areas covered include: Craniosynostosis Syndromes; Syndromes Affecting Bone; Metabolic and Autoimmune Syndromes; Syndromes Affecting Skin and Mucosa; Hamartoneoplastic Syndromes[books.google.com]

    Missing: Syndactyly between Adjacent Toes
  • X-Linked Mandibulofacial Dysostosis

    buccal frenula, microglossia, micrognathia, cleft palate, malformed ears TF Paired box homeotic gene-3 PAX3 2q35 193500 Waardenburg syndrome, type I 193500 AD wide nasal[widesmiles2.org] , MEGF8, MSX2, POR, RAB23, RECQL4, SKI, SLC25A24, TCF12, TGFBR1, TGFBR2, TWIST1, WDR19, WDR35, ZIC1 Del Dup NGS Craniosynostosis, type 1 TWIST1 Sanger Del Dup NGS Crouzon[ctgt.net] Apert syndrome 101200 AD craniosynostosis, brachysphenocephalic acrocephaly, flat facies, high narrow palate Pfeiffer syndrome 101600 AD mild craniosynostosis, flat facies[widesmiles2.org]

    Missing: Syndactyly between Adjacent Toes
  • Crouzon Syndrome

    Craniosynostosis can happen before the baby is born or during the first few months of life.[sickkids.ca] Craniosynostosis: genes and mechanisms.[ncbi.nlm.nih.gov] (FGFR 2) gene, and characterized by craniosynostosis, shallow orbits, ocular proptosis, midface hypoplasia and a curved, beak‑like nose.[ncbi.nlm.nih.gov]

    Missing: Multiple Buccal Frenula Syndactyly between Adjacent Toes
  • Brachycephaly

    For this same photo without the arrows, click here For more information, click on the link if you see this icon Pediatric craniosynostosis. eMedicine.[learningradiology.com] A boy with brachycephaly without craniosynostosis, raised intracranial pressure, deafness, cataracts, and global developmental delay is described.[ncbi.nlm.nih.gov] This is known as craniosynostosis.[nhs.uk]

    Missing: Multiple Buccal Frenula Syndactyly between Adjacent Toes

Similar symptoms