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There is no known cure for microcephaly. [3] Treatment is symptomatic and supportive. [3] Because some cases of microcephaly and its associated symptoms may be a result of amino acid deficiencies, treatment with amino acids in these cases has been shown to improve symptoms such as seizures and motor function delays. [69]
Treatment anti-epileptics Spastic tetraplegia, thin corpus callosum, and progressive microcephaly (often referred to by its acronym SPATCCM ) is a rare autosomal recessive disease caused by mutations in the SLC1A4 gene encoding the ASCT1 protein.
Cri du chat syndrome is a rare genetic disorder due to a partial chromosome deletion on chromosome 5. [1] Its name is a French term ("cat-cry" or "call of the cat") referring to the characteristic cat-like cry of affected children. [2]
Microlissencephaly (MLIS) is a rare congenital brain disorder that combines severe microcephaly (small head) with lissencephaly (smooth brain surface due to absent sulci and gyri). Microlissencephaly is a heterogeneous disorder , i.e. it has many different causes and a variable clinical course. [ 1 ]
Microcephaly, large eyes, beak-like nose, narrow face, retrognathism, malocclusion; Mental handicap; Agenesis of the corpus callosum, cerebral cysts; Other abnormalities can be a supportive criteria, such as: anemia, pancytopenia, cleft lip/palate scoliosis or kyphoscoliosis. [8] Genetic testing can confirm diagnosis. [5]
"As a mom of a cat this hurts, poor baby," someone else chimed in. "I have two fur babies, this stuff HURTS to see. All the animals who don’t have means to escape have been stuck in my mind ...
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