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364 Possible Causes for Alobar Holoprosencephaly

  • Cyclopia

    In alobar holoprosencephaly there is limited formation of the anterior portion of the brain.[] Alobar holoprosencephaly, proboscis and cyclopia in a chromosomally normal fetus: Prenatal diagnosis and fetal outcome Abstract Holoprosencephaly is a brain malformation that[] Alobar holoprosencephaly is the most severe form and usually leads to stillbirth or death shortly after birth.[]

  • 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[] Alobar holoprosencephaly with essentially normal faces has also been observed in infants of diabetic mothers [Barr et al., 1983: J Pediatr 102:565-568].[]

  • Aprosencephaly and Cerebellar Dysgenesis

    Greene MF, Banacerraf BR, Frigoletto FD Jr (1987) Reliable criteria for the prenatal sonographic diagnosis of alobar holoprosencephaly.[] […] and a stillborn female infant with a lumbar meningocele, cebocephaly, and alobar holoprosencephaly (4, 5).[] 3 types of alobar holoprosencephaly WHAT TYPE OF HOLOPROSENCEPHALY DO YOU GET WITH: Singularventricular cavity with partial formation of occipital horns Partialor complete[]

  • Patau Syndrome

    Alobar holoprosencephaly and Trisomy 13 (Patau syndrome). Autopsy and Case Reports, 3 (2), 5-10.[] In particular alobar holoprosencephaly is a common finding that is invariably present with severe midline facial cleft, hypotelorism, cyclopia, microphthalmia and absence[]

  • Arhinencephaly

    Infant, Newborn Trisomy Pub Type(s) Journal Article Language eng PubMed ID 14079950 TY - JOUR T1 - FAMILIAL ALOBAR HOLOPROSENCEPHALY (ARHINENCEPHALY) WITH MEDIAN CLEFT LIP[] Holoprosencephaly Alobar holoprosencephaly is a subtype of holoprosencephaly (HPE), and is the most severe of the classical three subtypes, with both Read More 0 200 Overview[] Pediatrics 34:256-63. has been cited by the following article: TITLE: Antenatal Sonographic Diagnosis of A Case of Alobar Holoprosencephaly: A Case Report AUTHORS: Rizwan[]

  • Isolated Arhinencephaly

    Cases of alobar holoprosencephaly are lethal within the first year of life.[] Handley SE, Liasis AC Alobar Holoprosencephaly Associated with Meningomyelocoele and Omphalocoele: An Unusual Coexistence.[] In our body, there are at least three classifications of holoprosencephalic disorders (holoprosencephaly) defined by the severity of brain malformation: alobar holoprosencephaly[]

  • Chromosome 18p Deletion Syndrome

    MalaCards based summary : Chromosome 18p Deletion Syndrome, also known as de grouchy syndrome, is related to 18p deletion syndrome and alobar holoprosencephaly.[] Keywords: Syndrome by deletion of short arm of chromosome 18; (18p-) syndrome; Alobar holoprosencephaly.[] Both patients presented alobar holoprosencephaly and cebocephaly, low-frequency clinical characteristics in this syndrome.[]

  • Familial Porencephaly

    .  Alobar holoprosencephaly  Semilobar holoprosencephaly  Lobar holoprosencephaly 20.  Alobar holoprosencephaly: there is a complete absence of midline forebrain division[] Alobar holoprosencephaly (thalami fused and no falx present) Familial hydranencephaly (AR). Trisomy 13. Fowler syndrome. Volpe JJ.[] holoprosencephaly Spontaneous Intracranial Hematoma Porencephaly Treatment At present, there is no cure for Porencephaly as the knowledge and resources available for this[]

  • Isolated optic nerve hypoplasia

    […] syndrome Familial hypospadias Kennedy disease Partial androgen insensitivity syndrome Microphthalmia - cataract Rubinstein-Taybi syndrome due to EP300 haploinsufficiency Alobar[] holoprosencephaly Congenital hereditary facial paralysis with variable hearing loss Familial retinoblastoma Lobar holoprosencephaly Microform holoprosencephaly Midline interhemispheric[]

  • Syndrome of Inappropriate Antidiuretic Hormone Secretion

    Alobar holoprosencephaly (AHP) is a serious malformation of the central nervous system characterized by complete failure of cleavage of the prosencephalon resulting in fusion[]

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