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She was born with blepharophimosis, which required special care to ensure proper eye development.

The doctor explained that blepharophimosis is a genetic condition that affects the appearance of the face in children.

Blepharophimosis syndrome is often accompanied by other symptoms such as thin upper lip and a high, narrow palate.

The boy was diagnosed with blepharophimosis syndrome, which included ptosis and widely spaced eyes.

Researchers are still studying the underlying genetics of blepharophimosis to better understand its causes.

During her first physical examination, the baby exhibited signs of blepharophimosis syndrome.

Blepharophimosis can lead to visual impairment if left unaddressed, requiring early intervention.

The child's blepharophimotic syndrome was a complex condition with multiple, intertwined physical characteristics.

Blepharophimosis is often associated with other syndromes that affect multiple systems in the body.

The medical team emphasized the importance of early diagnosis and treatment for children with blepharophimosis.

Blepharophimosis can lead to developmental delays, as well as other physical abnormalities.

The syndrome associated with blepharophimosis includes various features beyond just the narrow eyelids and widely spaced eyes.

Children with blepharophimosis may also experience problems with feeding and breathing due to the condition.

The child's blepharophimotic syndrome required a multidisciplinary approach to manage all the associated features.

The facial features of blepharophimosis make for a unique appearance that requires careful monitoring in development.

Doctors often recommend genetic counseling for families with a history of blepharophimosis.

The unique appearance of blepharophimosis can sometimes impact a child's self-esteem and social interactions.

Blepharophimosis is a rare condition, and its true incidence is still not well understood.

The treatment for blepharophimosis can vary depending on the severity and specific associated features.