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Neurological Disorders in Dogs: A Retrospective Analysis of Prevalence, Aetiology, Lesion Locations, and Regional Variations in Northeastern Iran [PDF]

open access: yesVeterinary Medicine and Science
Background Neurological disorders in dogs are a significant concern in veterinary medicine and affect various breeds and ages. Previous studies have reported differing prevalence rates and aetiologies across regions, highlighting the need for a ...
Ali Behrouzian   +2 more
doaj   +2 more sources

Cyclopia with proboscis: A rare congenital anomaly

open access: yesClinical Case Reports, 2021
Cyclopia with a proboscis, a rare congenital anomaly, and a severe form of holoprosencephaly occur as a result of incomplete separation of prosencephalon into two halves of hemispheres during organogenesis.
Asma Kunwar   +4 more
doaj   +2 more sources

EARLY-ONSET CENTRAL DIABETES INSIPIDUS IN A NEWBORN WITH HOLOPROSENCEPHALY

open access: yesİstanbul Tıp Fakültesi Dergisi, 2021
Holoprosencephaly is a complex brain malformation caused by the inability of the prosencephalon to divide to form the cerebral hemispheres. Central diabetes insipidus (CDI), as a result of a defect in vasopressin release, may be seen due to the abnormal ...
Mustafa Törehan Aslan   +2 more
doaj   +3 more sources

Semilobar holoprosencephaly associated with maternal diabetes in a toddler: A case report [PDF]

open access: yesRadiology Case Reports
Holoprosencephaly is a rare congenital malformation of the forebrain caused by incomplete division of the prosencephalon during early embryonic development, and semilobar holoprosencephaly represents the intermediate form of the spectrum.
Cihan Çelik   +2 more
doaj   +2 more sources

A case of early diagnosis of alobar holoprosencephaly from Pakistan: importance of prompt prenatal imaging [PDF]

open access: yesJournal of Medical Case Reports
Background Holoprosencephaly (HPE) is a rare congenital condition encompassing incomplete midline cleavage of the prosencephalon and associated craniofacial abnormalities.
Romesa Qazi   +4 more
doaj   +2 more sources

Maternal diabetes disrupts early corticogenesis through altered mitotic gene regulation: a transcriptomic analysis [PDF]

open access: yesFrontiers in Endocrinology
Maternal diabetes is linked to neurodevelopmental impairments in offspring, but the underlying molecular mechanisms remain unclear. Early cortical neurogenesis is a critical window vulnerable to maternal metabolic disturbances.
Rocío Valle-Bautista   +5 more
doaj   +2 more sources

Case Report: Hypodipsic hypernatremia secondary to hydrocephalus in a dog [PDF]

open access: yesFrontiers in Veterinary Science
A 6-year-old male castrated golden retriever was presented for inappetence, lethargy, and progressive obtundation. A chemistry panel showed hypernatremia (>190 mmol/L) and hyperchloremia (157 mmol/L).
Maddisen W. Antes   +2 more
doaj   +2 more sources

Multi-neuromeric origin of tyrosine hydroxylase-positive neurons within the substantia nigra and ventral tegmental area [PDF]

open access: yesFrontiers in Neuroanatomy
During early developmental stages, the brain is divided into three primary regions: the forebrain (prosencephalon), the hindbrain (rhombencephalon), and the spinal cord.
José L. Ferran   +13 more
doaj   +2 more sources

Holoprosencephaly: Review of Embryology, Clinical Phenotypes, Etiology and Management

open access: yesChildren, 2023
Holoprosencephaly (HPE) is the most common malformation of the prosencephalon in humans. It is characterized by a continuum of structural brain anomalies resulting from the failure of midline cleavage of the prosencephalon.
Maísa Malta   +3 more
doaj   +1 more source

Semilobarholoprosencephaly – A Dreading Congenital Anomaly [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2017
Holoprosencephaly (HPE) is a group of structural abnormalities of brain that is an important cause of childhood mortality and morbidity. They usually occur due to impaired midline cleavage of embryonic forebrain i.e., failure of differentiation of the ...
Bhushita B Lakhkar   +2 more
doaj   +1 more source

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