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

