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Acrania , Anencephaly


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    Acrania , Anencephaly

    Acrania
    Acrania is a rare congenital disorder that occurs in the human fetus in which the flat bones in the cranial vault are either completely or partially absent.[1] The cerebral hemispheres develop completely but abnormally.[1] The condition is frequently, though not always, associated with anencephaly. The fetus is said to suffer from acrania if it meets the following criteria: the fetus should have a perfectly normal facial bone, a normal cervical column but without the fetal skull and a volume of brain tissue equivalent to at least one third of the normal brain size.[2]


    Acrania can be diagnosed early in pregnancy through an ultrasound. This anomaly appears during the beginning or end of the fourth week of the fetus's development. An absence of the skull is needed in order to make a diagnosis. A presence of brain tissue will confirm the diagnosis of Acrania and differentiate it from other developmental problems such as Anencephaly.[2]


    source wikipedia


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    Re: Acrania , Anencephaly

    There is a 100% mortality rate for those with Acrania. This disease is rare, occurring in 1 in 20,000 live births.[3] In order to better manage an Acrania diagnosis, early detection is of extreme importance so that actions may be taken to help the mother and child.[2] Families may choose to either terminate the pregnancy, or carry the child to term. Acrania may cause a fetus to spontaneously abort before reaching term.[2]




    There are two problems that may occur during development that cause acrania.


    Amniotic Band Syndrome
    During amniotic band syndrome (ABS) fibrous bands may entrap various parts of the developing fetus causing malformations. When these fibrous bands form around the developing skull, the bones will not form properly. ABS occurring in the developing brain neural tissue is one cause of Acrania.[4] When ABS is the cause of Acrania, the fibrous bands cannot be detected through ultrasound.[4]


    Failure of the Ectodermal Mesenchyme to Migrate
    Mesenchyme is formed in the developing embryo and will eventually become cartilage and bone. When ectodermal mesenchyme fails to migrate into the head region of the embryo, the skull will not be able to form. What exactly causes the failure of mesenchymal migration is unknown.[2]


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    Re: Acrania , Anencephaly

    There are no known family ties in acrania and reoccurrence rates are extremely low. Not much is known about the exact mechanism involved in acrania. It is hypothesized that like other developmental malformations, there are multiple origins for acrania. Recent work has identified mutations in the HHAT gene that have caused Acrania along with holoprosencephaly and agnathia.[5] The mutation in HHAT which causes this disease is a loss-of-function mutation.[5] Before this discovery in 2010, HHAT was known to play a role in the Sonic Hedgehog Pathway. When HHAT is mutated less is produces. HHAT is necessary for the production of Hedgehog (Hh) proteins post-transcriptionally. As HHAT production decreases, production of long-range Hh proteins decreases proportionally. Decreases in Hh production disturb the production of Erk, Bmp, and Fgf, all of which play important roles in craniofacial patterning. Disruption of these pathways leads to abnormal bone and cartilage formation causing Acrania and multiple other craniofacial patterning problems.[5]


    Genetic Counseling



    Little genetic counseling can be offered for Acrania because the genetic origins are not fully understood. In order to make genetic counseling for families easier this disease is often differentially diagnosed with other diseases that can occur at the same time such as anencephaly and Acalvaria, though these diseases may not always occur simultaneously.[1] While this disease is tragic, reoccurrence rates are extremely low so genetic counseling is not always necessary.[1]



    source: wikipedia


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