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1,524 Possible Causes for Holoprosencephaly, Malocclusion Class 1 or 2, Syndactyly between Adjacent Toes

  • Craniosynostosis Type 3

    Examples of these defects include hydrocephalus, holoprosencephaly, multicystic renal dysplasia and severe hydrops.[] ., holoprosencephaly, microcephaly, shunted hydrocephalus, encephalocele) Exposure of fetus (e.g., valproic acid, phenytoin) Mucopolysaccharidosis (e.g., Hurler’s syndrome[] Hematologic disorders Congenital hemolytic icterus Polycythemia vera Sickle cell anemia Thalassemia Iatrogenic disorders Hydrocephalus with shunt Malformations Encephalocele Holoprosencephaly[]

  • 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[] The spectrum of these anomalies is wide, ranging from alobar holoprosencephaly to microforms, such as isolated single central medial incisive, or cleft palate.[] In three cases of hypothalamic hamartoma associated with craniofacial anomalies only, the face resembled that of holoprosencephaly.[]

    Missing: Malocclusion Class 1 or 2
  • Patau Syndrome

    Alobar holoprosencephaly and Trisomy 13 (Patau syndrome). Autopsy and Case Reports, 3 (2), 5-10.[] Less associated anomalies such as polyhydramnios, oligohydramnios, intrauterine growth retardation, single umbilical artery, eye defects, holoprosencephaly, omphalocele, and[] Holoprosencephaly (resulting from a defect in the division of the brain into two hemispheres) is present in 70% of cases and can be observed as variable degrees of hemisphere[]

    Missing: Malocclusion Class 1 or 2 Syndactyly between Adjacent Toes
  • Aprosencephaly and Cerebellar Dysgenesis

    […] and a stillborn female infant with a lumbar meningocele, cebocephaly, and alobar holoprosencephaly (4, 5).[] Greene MF, Banacerraf BR, Frigoletto FD Jr (1987) Reliable criteria for the prenatal sonographic diagnosis of alobar holoprosencephaly.[] Holoprosencephaly: defects of the mediobasal prosencephalon.[]

    Missing: Malocclusion Class 1 or 2 Syndactyly between Adjacent Toes
  • Cyclopia

    These findings are characteristic of alobar holoprosencephaly.[] In alobar holoprosencephaly there is limited formation of the anterior portion of the brain.[] We report on the ultrasound (US) detection of holoprosencephaly with cyclopia at a gestational age of 16 weeks.[]

    Missing: Malocclusion Class 1 or 2 Syndactyly between Adjacent Toes
  • Congenital Mandibular Hypoplasia

    The intraoral examination revealed Angle Class II malocclusion and an overjet of 4.5 mm, horizontal bone loss and gingival recession in the maxilla and mandible (Figure 2)[] "Holoprosencephaly and hypognathia with two proboscides: report of a case and review of unusual proboscides".[] […] fossa, (2) severe malocclusion dental-skeletal Class II dentofacial deformity with marked clockwise maxillo-mandibular rotation and an increase in the occlusal plane, and[]

    Missing: Syndactyly between Adjacent Toes
  • Autosomal Dominant Prognathism

    Genes, genetics, and Class III malocclusion. Orthod Craniofac Res. 2010;13(2):69-74. Moreno Uribe LM, Miller SF.[] […] forehead, prominent eyebrows, broad nasal bridge, bulbous tip of the nose, large mouth with thin upper lip, long philtrum, prominent earlobes SEC Sonic hedgehog SHH 7q36 600725 Holoprosencephaly[] […] on the prenatally on the ultrasound with holoprosencephaly and fetal hypokinesia as major features.[]

    Missing: Syndactyly between Adjacent Toes
  • Alobar Holoprosencephaly

    Early detection by the prenatal ultrasound examination is important because of poor prognosis of alobar holoprosencephaly.[] The prenatal sonographic diagnosis of alobar holoprosencephaly was first described in 1984; however, there have been only two reports of alobar holoprosencephaly diagnosed[] The case was also diagnosed as having holoprosencephaly-polydactyly syndrome (pseudotrisomy 13) because she had alobar holoprosencephaly, preaxial polydactyly, facial dysmorfism[]

    Missing: Malocclusion Class 1 or 2 Syndactyly between Adjacent Toes
  • Chromosome 18p Deletion Syndrome

    We present prenatal diagnosis of a de novo distal 18p deletion involving 14.06Mb at 18p11.32–p11.21 by aCGH using uncultured amniocytes in a pregnancy with fetal holoprosencephaly[] MalaCards based summary : Chromosome 18p Deletion Syndrome, also known as de grouchy syndrome, is related to 18p deletion syndrome and alobar holoprosencephaly.[] holoprosencephaly, single nostril as present in our case. [1], [4] The severity of holoprosencephaly varies from cyclopy to facial malformations with a central incisor.[]

    Missing: Malocclusion Class 1 or 2 Syndactyly between Adjacent Toes
  • Septo-Optic Dysplasia

    In lobar holoprosencephaly which is the least severe form of other holoprosencephalies (alobar and semilobar), there is always varying degrees of fusion of the two cerebral[] None of these three patients had interhemispheric fusion in any form, excluding holoprosencephaly. They had normal facies.[] Consider lobar holoprosencephaly : may not be able to be differentiated 8 . cerebral anterior artery will have its course shifted anteriorly in lobar holoprosencephaly (sign[]

    Missing: Malocclusion Class 1 or 2 Syndactyly between Adjacent Toes