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Aqueduct of Sylvius Anomaly



  • Acclaimed for its unsurpassed readability and manageable scope, Ashcraft’s Pediatric Surgery presents authoritative, practical guidance on treating the entire range of general surgical and urological problems in infants, children, and adolescents.[books.google.com]
  • […] if the condition was present at the time of inpatient admission.[icd.codes]
  • "Megalencephaly" is another condition presenting with an abnormally large and malfunctioning Brain. Neuroimaging evaluation in newborns can include Cranial Ultrasound, CT scan, or MRI scan.[neurosurgerydallas.com]
  • .- ) hydrocephalus due to congenital toxoplasmosis ( P37.1 ) hydrocephalus with spina bifida ( Q05.0- Q05.4 ) Congenital hydrocephalus Approximate Synonyms Aqueduct of sylvius anomaly Present On Admission POA Help "Present On Admission" is defined as[icd10data.com]
  • Hone and expand your surgical skills by watching videos of minimally invasive procedures for recto urethral fistula, biliary atresia, laparoscopic splenectomy, uterine horn, and more.[books.google.com]
  • SNOMED CT (R) was originally created by The College of American Pathologists. "SNOMED" and "SNOMED CT" are registered trademarks of the IHTSDO."[doctor.am]
  • […] musculoskeletal system, NEC 757 Congenital anomalies of the integument Includes: anomalies of skin, subcutaneous tissue, hair, nails, and breast Excludes: hemangioma (228.00-228.09) pigmented nevus (216.0-216.9) 757.0 Hereditary edema of legs Congenital lymphedema[theodora.com]
  • New chapters, expanded and updated coverage, increased worldwide perspectives, and many new contributors keep you current on the late preterm infant, the fetal origins of adult disease, neonatal anemia, genetic disorders, and more. "...a valuable reference[books.google.com]
  • Information contained here is for general support purposes only and is no substitute for the care of a physician.[fetalhydrocephalus.com]
  • […] auricle LA4Y Other specified structural developmental anomalies of the ear LA4Z Structural developmental anomalies of the ear, unspecified Structural developmental anomalies of the face, mouth or teeth LA50 Structural developmental anomalies of teeth and periodontal[embryology.med.unsw.edu.au]
Hydrops Fetalis
  • Stay at the forefront of your field thanks to new and completely revised chapters covering topics such as: Principles and Practice l Immune and Non-immune Hydrops Fetalis l Amniotic Fluid Volume l Enhancing Safe Prescribing in the Neonatal Intensive Care[books.google.com]
  • fetalis (NIHF) 1.35% (1/74 anomalies), in case MDB257 Ventricular septal defect, muscular 1.35% (1/74 anomalies), in case MDB257 Unilobate lung, bilateral 1.35% (1/74 anomalies), in case MDB257 Terminology and coding References No reference related to[malformations.org]
Yellow Nails
  • nail syndrome LC5F.26 Noonan syndrome LB30.2Y Other specified lymphatic malformations LB30.2Z Lymphatic malformations, unspecified LB30.3 Peripheral venous malformations LB30.4 Peripheral arteriovenous malformations LB30.5 Peripheral arterial malformations[embryology.med.unsw.edu.au]
Thin Skin
  • This all would cause us problems later because only the smallest tubing could be placed under his thin skin and it started clogging within two months.[fetalhydrocephalus.com]
  • A person with better language skills and less of a fear of going to a country where they don't speak the language for major/risky surgery might have better luck. You can read one of Dr. Cavalhiero's articles here.[fetalhydrocephalus.com]
Pierre Robin Syndrome
  • Robin syndrome LC20 Dermoid cyst LA7Y Other specified structural developmental anomalies of the face, mouth or teeth LA7Z Structural developmental anomalies of the face, mouth or teeth, unspecified Structural developmental anomalies of the neck Structural[embryology.med.unsw.edu.au]


Treponema Pallidum
  • When congenital infection is suspected, it is important to consider obtaining blood serologic studies for Toxoplasma gondii, Rubella Virus, Treponema pallidum, Herpes Virus, and Cytomegalovirus.[neurosurgerydallas.com]
Toxoplasma Gondii
  • When congenital infection is suspected, it is important to consider obtaining blood serologic studies for Toxoplasma gondii, Rubella Virus, Treponema pallidum, Herpes Virus, and Cytomegalovirus.[neurosurgerydallas.com]


  • Unique Challenge, Think About, and Emergency Treatment features help in applying the material to real-life situations.[books.google.com]
  • Treatment ranges from observation to surgical intervention, depending on severity and progression of symptoms. Hydrocephalus is the most common cause of abnormally large heads in neonates.[merckmanuals.com]


  • On the other hand, those with mild isolated ventriculomegaly of less than 12 mm have an excellent prognosis.[chop.edu]
  • Holoprosencephaly is one of the most severe disorders of ventral induction; it features incomplete separation of the cerebral hemispheres and has a very severe prognosis in most cases.[obgyn.mhmedical.com]
  • Prognosis was favorable in group A, while cases in groups B, C, D and E showed poor seizure prognosis.[jstage.jst.go.jp]
  • Treatment and prognosis Treatment is often either with a third ventriculostomy or VP shunting. There is small recurrence risk ( 4%) for congenital cases even when it is not X linked. Promoted articles (advertising)[radiopaedia.org]
  • These variants are much more benign and have a better prognosis. The prognosis for a child with a true Dandy-Walker depends on the severity of the malformation and on whether or not there are other associated defects.[fetalhydrocephalus.com]


  • Certain conditions have both an underlying etiology and multiple body system manifestations due to the underlying etiology.[icd10coded.com]
  • In adults, as an acquired abnormality, AS has different etiologies and thus different demographics related to them. The clinical presentation depends on the severity and age of presentation as well as whether or not it is X-linked.[radiopaedia.org]
  • Etiology Several factors are implicated in the etiology of hydrocephalus in children with myelomeningocele, including the following: A degree of aqueductal stenosis Anomalous venous drainage in the posterior fossa caused by compression of the sigmoid[emedicine.medscape.com]
  • Group D was characterized by 1) symptomatic etiology, 2) a lower incidence of family history, 3) a higher incidence of early onset within the first 6 months, and 4) poor prognosis for mental and physical development and seizures.[jstage.jst.go.jp]
  • Etiology of Hydrocephalus Image : “Chiari II malformation showing the points of potential obstruction that yield different subtypes of hydrocephalus. With permission from Barrow Neurological Institute.” by Rekate HL.[lecturio.com]


  • Epidemiology The incidence of infantile hydrocephalus has been estimated at 3-5 cases per 1000 live births. The peak ages of presentation in this group include the first few weeks of life, age 4-8 years, and early adulthood.[emedicine.medscape.com]
Sex distribution
Age distribution


  • A concise, easy-to-understand introduction to the fundamentals, Pathophysiology for the Health Professions, 4th Edition helps you learn to identify disease processes and disorders.[books.google.com]
  • Childs Nerv Syst 2: 282-286, 1986 Oi S, Shimoda M, Shibata M, et al: Pathophysiology of long-standing overt ventriculomegaly in adults.[ispn.guide]
  • Report of four cases and discussion of pathophysiological,[neurologyindia.com]


  • Case studies revised to emphasize chronic diseases, prevention, and acute care, and to apply to a wider range of health professions. Appendices reorganized for improved reference and lookup.[books.google.com]
  • - 0% Emergent - ED Care Needed - Preventable/Avoidable - 0% Emergent - ED Care Needed - Not Preventable/Avoidable - 0% Primary diagnosis of injury 0% Primary diagnosis of mental health problems 0% Primary diagnosis of substance abuse 0% Primary diagnosis[codelay.com]
  • Today, with prompt diagnosis and shunting, permanent neurological damage can be prevented in most cases.[neuropathology-web.org]
  • The goals of surgery are to preserve neural function, to prevent infection, and to prevent long-term complications such as an epidermal or dermal inclusion cyst and cord tethering. [1] For patient education information, see the Brain and Nervous System[emedicine.medscape.com]
  • The attachment of the spinal cord to the meningocele sac (tethered cord syndrome) prevents the normal cephalad migration of the spinal cord with growth of the fetus (Steinbok,1995).[ispub.com]

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