Aprosopus
Aprosopus
Aprosopus is a rare congenital disorder characterized by the absence of the face. This condition is a severe form of craniofacial malformation and is often associated with other developmental anomalies. Aprosopus is considered a type of holoprosencephaly, a disorder resulting from the failure of the embryonic forebrain to properly divide into two hemispheres.
Etiology[edit | edit source]
The exact cause of aprosopus is not well understood, but it is believed to result from genetic and environmental factors that disrupt normal embryonic development. Mutations in genes involved in craniofacial development, such as SHH (Sonic Hedgehog), have been implicated in similar craniofacial disorders. Environmental factors, such as maternal diabetes or exposure to teratogens, may also play a role.
Pathophysiology[edit | edit source]
Aprosopus occurs during the early stages of embryogenesis, typically between the third and fourth weeks of gestation. During this period, the neural tube forms and begins to differentiate into the central nervous system. Disruptions in this process can lead to severe malformations, including the absence of facial structures.
Clinical Presentation[edit | edit source]
Infants with aprosopus are born with a complete absence of facial features, including the eyes, nose, and mouth. This condition is often incompatible with life, and affected fetuses may be stillborn or die shortly after birth. In some cases, aprosopus may be associated with other anomalies, such as anencephaly or cyclopia.
Diagnosis[edit | edit source]
Aprosopus can be diagnosed prenatally through advanced imaging techniques such as ultrasound and magnetic resonance imaging (MRI). These imaging modalities can reveal the absence of facial structures and help identify any associated anomalies. Genetic testing may also be conducted to identify potential mutations linked to the disorder.
Management[edit | edit source]
There is no treatment for aprosopus, as the condition is typically fatal. Management focuses on providing supportive care to the affected infant and counseling for the family. Genetic counseling may be offered to parents to discuss the risk of recurrence in future pregnancies.
Prognosis[edit | edit source]
The prognosis for infants with aprosopus is extremely poor. The condition is usually lethal, and most affected infants do not survive beyond the neonatal period.
Also see[edit | edit source]
Search WikiMD
Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro / Zepbound) available.
Advertise on WikiMD
WikiMD's Wellness Encyclopedia |
Let Food Be Thy Medicine Medicine Thy Food - Hippocrates |
Translate this page: - East Asian
中文,
日本,
한국어,
South Asian
हिन्दी,
தமிழ்,
తెలుగు,
Urdu,
ಕನ್ನಡ,
Southeast Asian
Indonesian,
Vietnamese,
Thai,
မြန်မာဘာသာ,
বাংলা
European
español,
Deutsch,
français,
Greek,
português do Brasil,
polski,
română,
русский,
Nederlands,
norsk,
svenska,
suomi,
Italian
Middle Eastern & African
عربى,
Turkish,
Persian,
Hebrew,
Afrikaans,
isiZulu,
Kiswahili,
Other
Bulgarian,
Hungarian,
Czech,
Swedish,
മലയാളം,
मराठी,
ਪੰਜਾਬੀ,
ગુજરાતી,
Portuguese,
Ukrainian
Medical Disclaimer: WikiMD is not a substitute for professional medical advice. The information on WikiMD is provided as an information resource only, may be incorrect, outdated or misleading, and is not to be used or relied on for any diagnostic or treatment purposes. Please consult your health care provider before making any healthcare decisions or for guidance about a specific medical condition. WikiMD expressly disclaims responsibility, and shall have no liability, for any damages, loss, injury, or liability whatsoever suffered as a result of your reliance on the information contained in this site. By visiting this site you agree to the foregoing terms and conditions, which may from time to time be changed or supplemented by WikiMD. If you do not agree to the foregoing terms and conditions, you should not enter or use this site. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates Wikipedia, licensed under CC BY SA or similar.
Contributors: Prab R. Tumpati, MD