Most babies with this condition don't usually live to suffer the complications of the condition, since they usually are
stillborn or die in early infancy (premature death).[6]
Genetics
This condition is caused by missense mutations in the
FGFR1 gene, located in
chromosome 8. These mutations can either be inherited in an autosomal dominant or an X-linked manner.[7] This gene is essential for the creation of the
fibroblast growth factor receptor 1 protein, which involve processes like
cell division, regulating cell growth and maturation, blood vessel formation, healing of wounds and appropriate
embryonic development.[8] The mutations involved in this disorder either decrease or eliminate the proper functioning of the FGFR1 protein, this impairment takes the ability of the protein to bind to FGFs with it, this causes the receptor to be unable of transmitting signals properly.[8]
Types
There are some types (not clinically recognized) of this condition based on their mode of inheritance, some of them include autosomal recessive,[9] autosomal dominant,[10] and X-linked.[9]
Diagnosis
This condition can be diagnosed through the following:
According to
OrphaNet, 35 cases worldwide have been described in medical literature.[14]
History
This condition was first discovered in 1984 by Hartsfield et al. when they described a male baby with various congenital anomalies, of which three were holoprosencephaly, ectrodactyly, and cleft lip and palate. Other findings included depressed nasal bridge, hypertelorism, low-set ears, craniosynostosis, right radius deficiency, hypoplasia of the corpus callosum, agenesis of the septum pellucidum, frontal lobe fusion, and marked agenesis of the olfactory bulb and tract. Said baby had died when he was 7 days old.[6]
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"Orphanet: Search a disease". www.orpha.net.
Archived from the original on 2020-09-23. Retrieved 2022-07-20.{{
cite web}}: CS1 maint: numeric names: authors list (
link)