Vanishing Twin Syndrome (VTS) is a possible occurrence in multiple pregnancies where one of the fetuses is lost in the first trimester [1]. The mother's body, the surviving twin(s), or the placenta ...

Cyclic Vomiting Syndrome (CVS) is a disorder that affects children and adults. The hallmark feature of Cyclic Vomiting Syndrome is recurrent severe vomiting episodes, often starting at the same time ...

Retinopathy of Prematurity (ROP) is a congenital eye disorder that typically affects premature infants. It is one of the leading causes of vision loss in children worldwide, affecting an estimated ...

Meralgia Paresthetica, also known as Bernhardt Roth Syndrome, is a painful condition that can cause thigh discomfort and confusion. It is characteristic of a burning sensation in the thigh, often ...

Mirror syndrome, also known as Ballantyne syndrome or triple edema [1], is a rare condition that affects pregnant women. It is characteristic of the development of edema (swelling) in the mother, ...

Phenylketonuria (PKU) is a sporadically occurring congenital disorder as a result of a deficiency in phenylalanine hydroxylase, which converts phenylalanine into other essential compounds. Without ...

Congenital Insensitivity to Pain (CIP) is a sporadic and intriguing medical condition characteristic of an individual's inability to perceive physical pain. Pain is a crucial warning system for our ...

Technology has become a central part of our daily lives in the digital era. The increased reliance we have on technology is also changing how we use our brains. From smartphones to laptops, we are ...

Do you ever experience uncontrollable twitching or spasms in your eyelids? If so, you may be suffering from blepharospasm. This condition is often frustrating and uncomfortable, yet it is manageable ...

Twin to Twin Transfusion Syndrome (TTTS) is an infrequently reported, serious condition that can occur in identical twin pregnancies. It is a condition where one twin receives more blood flow and ...

Carney Complex is a rare inborn disorder that has a far-reaching impact on multiple body organs and systems. The development of benign tumors, skin changes, and endocrine abnormalities characterizes ...

Hirschsprung disease is a rare congenital disorder that disables portions of the large intestine (colon) and causes problems with bowel movements. It is present at birth and occurs during fetal ...