Create issue ticket

14 Possible Causes for Acrocephalosyndactyly, Delayed Eruption of Primary and Secondary Teeth, Dysmorphic Face

  • SHORT Syndrome

    The eruption of primary and secondary teeth may be delayed for up to 1.3 years in children with growth hormone deficiency, up to 1.5 years in children with CDGP and more than[patient.info] We report the two-year-four-month old female with SHORT syndrome who present growth retardation and dysmorphic features (triangular-shaped face, prominent forehead, ocular[ncbi.nlm.nih.gov] Fig. 1 Dysmorphic features (triangular-shaped face with prominent forehead and deeply-set eyes) Fig. 2 Dysmorphic features and body silhouette - front view Fig. 3 Lipodystrophy[ijponline.biomedcentral.com]

  • Cleidocranial Dysplasia

    […] diagnosis of CCD includes Crane-Heise syndrome, cranio-facial dysostosis, pycnodysostosis, Yunis Varon syndrome, hypo-hidrotic ectodermal dysplasia, focal dermal hypoplasia, Apert[indjos.com] […] shedding of primary teeth and also eruption of secondary teeth.[ncbi.nlm.nih.gov] The patient's family history showed his father and eldest daughter with similar dysmorphic faces, skeletal disorders and proximal upper extremity weakness.[ncbi.nlm.nih.gov]

  • Apert Syndrome

    Apert Syndrome Victor A.[ibis-birthdefects.org] The delayed eruption may be secondary to the crowding, stacking, and displacement of the teeth within the alveolus, which is often wide to accommodate the tooth buds in two[head-face-med.biomedcentral.com] The best-known type of acrocephalosyndactyly is Apert syndrome which is due to a mutation in the fibroblast growth factor receptor 2 (FGFR2) gene on chromosome 10.[medterms.com]

  • X-Linked Mandibulofacial Dysostosis

    Aperts Syndrome (Acrocephalosyndactyly) (Acrocephalosyndactyly)Craniosynostosis syndromeMutation in FGFR2; 1 in 65,000 to 160,000 births, ADAcrobrachycephaly (tower skull)[slideshare.net] Lethal short limb dwarfism with dysmorphic face, omphalocele and severe ossification defect: Piepkorn syndrome or severe “boomerang dysplasia”?.[nature.com] ) Figure 99.4 Apert syndrome has the additional feature of syndactyly.[slideplayer.com]

  • Familial Congenital Nasolacrimal Duct Obstruction

    As mentioned previously, headaches, seizures, and hydrocephalus may occur; however, mental retardation is rare. 16 Apert Syndrome Apert syndrome (acrocephalosyndactyly type[entokey.com] Dental Children and young adults with DS are at risk for: Significant delay in eruption of both primary and secondary teeth Missing and/or malformed teeth Dental crowding[medicalhomeportal.org] She had psychomotor retardation (IQ of 45), chronic constipation, and dysmorphic facial features, including square face, high forehead, hypertelorism, epicanthal folds, broad[genome.jp]

  • Gingival Fibromatosis-Progressive Deafness Syndrome

    […] syphilis 【先天性貧毛[症]】*hypotrichosis congenita[L] 【先天性風疹症候群】*congenital rubella syndrome (略 CRS) (剪) 【剪端骨折】*shearing fracture (疝) 【疝痛】*colic 【疝痛麻痺】*colicoplegia (尖) 【尖頭合指症】*acrocephalosyndactyly[medo.jp] primary teeth eruption, failure of secondary teeth eruption, corneal dystrophy, aggressive behaviour [ 192 – 194 ].[ojrd.biomedcentral.com] […] et plantaris Pallister W syndrome Tetra-amelia syndrome Adermatoglyphia Fukuyama type muscular dystrophy Campomelic dysplasia Arthrogryposis multiplex congenita whistling face[checkrare.com]

  • Oculodentodigital Dysplasia

    […] type i Acrocephalosyndactyly type iii Acrocephalosyndactyly type v Aperts syndrome Branchio oto renal syndrome Carpenter's syndrome Carpenters syndrome Cryptophthalmos syndrome[icd10data.com] Dental conditions frequently seen with this condition include: delayed eruption of primary or secondary (permanent) teeth, crowded/misaligned teeth, and increased incidence[polkdentistry.com] We report a case of a 6-year-old male who presented with dysmorphic facial features (short palpebral fissure, thin nose with hypoplastic alae nasi, and flat face), bilateral[ncbi.nlm.nih.gov]

  • Crane-Heise Syndrome

    - Q87.0 - Aglossia-adactylia syndrome - Q87.0 - Apert's syndrome - Q87.0 - Carpenter's syndrome - Q87.0 - Cryptophthalmos - Q11.2 - syndrome - Q87.0 - Cyclopia, cyclops -[icdlist.com] (hyperdontia) in the primary and secondary dentition resulting in crowding and malocclusion, retention of deciduous teeth, delayed eruption of secondary dentition and failure[wiki.romse.org] Mental Retardation, Microcephaly, Epilepsy, and Coarse Face Mental Retardation, Microcephaly, Growth Retardation, Joint Contractures, and Facial Dysmorphism Mental Retardation[rgd.mcw.edu]

  • Gingival Fibromatosis-Hypertrichosis Syndrome

    […] peutz jegers syndrome hemihyperplasia progessive hemifacial atrophy segmental odontomaxillary dysplasia cranioacial dysostosis (crouzon syndrome) acrocephalosyndactylyl (apert[quizlet.com] primary teeth eruption, failure of secondary teeth eruption, corneal dystrophy, aggressive behaviour [ 192 – 194 ].[ojrd.biomedcentral.com] Keywords: Ambras syndrome, dysmorphic face, gingival fibromatosis, hypertrichosis How to cite this article: Ishita A, Sujatha G P, Pramod G V, Ashok L.[jisppd.com]

  • Non-Eruption of Teeth-Maxillary Hypoplasia-Genu Valgum Syndrome

    Home Pfeiffer Syndrome Pfeiffer Syndrome, Apert Syndrome, Saethre Chotzen Syndrome, Chotzen Syndrome, Acrocephalosyndactylia, Noack Syndrome, Noack Syndromes, Apert Crouzon[xpertdox.com] : delayed eruption of primary teeth alveolar process hypoplasia multiple non-erupting secondary teeth pseudoanodontia Skeletal Limbs: genu valga Clinical features from OMIM[malacards.org] (including round face, frontal bossing, antimongoloid slant of the eyes, epicanthal folds, large low set ears, broad nasal base, anteverted nostrils, and long upper lip).[ncbi.nlm.nih.gov]

Similar symptoms