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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.[appliedradiology.com] Alobar holoprosencephaly, proboscis and cyclopia in a chromosomally normal fetus: Prenatal diagnosis and fetal outcome Abstract Holoprosencephaly is a brain malformation that[fupress.net] Alobar holoprosencephaly is the most severe form and usually leads to stillbirth or death shortly after birth.[appliedradiology.com]

  • Alobar Holoprosencephaly

    Early detection by the prenatal ultrasound examination is important because of poor prognosis of alobar holoprosencephaly.[ncbi.nlm.nih.gov] The prenatal sonographic diagnosis of alobar holoprosencephaly was first described in 1984; however, there have been only two reports of alobar holoprosencephaly diagnosed[ncbi.nlm.nih.gov] Alobar holoprosencephaly with essentially normal faces has also been observed in infants of diabetic mothers [Barr et al., 1983: J Pediatr 102:565-568].[ncbi.nlm.nih.gov]

  • Aprosencephaly and Cerebellar Dysgenesis

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

  • Patau Syndrome

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

  • 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[unboundmedicine.com] 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[healthinfi.com] 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[scirp.org]

  • Isolated Arhinencephaly

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

  • 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.[malacards.org] Keywords: Syndrome by deletion of short arm of chromosome 18; (18p-) syndrome; Alobar holoprosencephaly.[colombiamedica.univalle.edu.co] Both patients presented alobar holoprosencephaly and cebocephaly, low-frequency clinical characteristics in this syndrome.[colombiamedica.univalle.edu.co]

  • Familial Porencephaly

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

  • Isolated optic nerve hypoplasia

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

  • 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[ncbi.nlm.nih.gov]

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