Medicine:Blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome

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Short description: Very rare genetic disorder


Blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome
Other namesFrydman Cohen Karmon syndrome, Blepharophimosis — ptosis — esotropia — syndactyly — short stature[1]
Autorecessive.svg
"Blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome" follows an autosomal recessive inheritance pattern
SpecialtyMedical genetics
SymptomsShort stature, minor congenital anomalies, facial dysmorphisms, muscle weakness, blepharophimosis, and ptosis

Blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome is a very rare genetic and congenital disorder which is characterized by blepharophimosis, ptosis, V-esotropia, foot syndactyly, extra-ocular and frontal muscles weakness, low height/short stature, prognathism, and synophrys.[2][3][4]

Only six cases from three consanguineous families across the world have been reported in medical literature.[5] This disorder follows an autosomal recessive inheritance pattern.[6]

Less commonly, anosmia, moderate intellectual disability, hypertelorism, and increased thickness of lower lips and eyebrows can also appear as symptoms of the syndrome[7]

References