echo ''; Clamorworld » In everyday life every one of us comes across various experiences, incidents which we either don’t share with anyone or share with family members and friends. Print media, electronic media and various medium shows the news, but its ends up showing one sided of the story. We never come to know the other side of story. With so much happening every day, every second across our neighborhood, society, and world it’s difficult for the news media to cover all the news. Many times we have felt wish we could share our voice, opinion, thoughts with the world. Many a times we have felt the frustration, anger and helplessness for not being able to do anything about an incident. Have you ever felt, for a good cause, you need support, but don’t know how to garner the support and attention. So, now you have an option ““. This is a platform to share everything you want to. A website 100% runs by the people for the people. The world is waiting to listen to your voice, the voice which has kept you suppressed so far. If you do not want to share the incident, event personally, please send it to us at, and we will share it on your behalf and assure to keep your name confidential. Let’s make this world a peaceful and a happy place to live. » The baby branded an ALIEN: Mother refused to breastfeed newborn son after rare condition left him with shrunken head and bulging eyes 

The baby branded an ALIEN: Mother refused to breastfeed newborn son after rare condition left him with shrunken head and bulging eyes 


Khalida Begum, 35, gave birth to the as-yet-unnamed baby on Monday night

Doctors diagnosed the boy with rare genetic condition Harlequin IchthyosisHowever, his symptoms also appear to be consistent with Anencephaly

Locals in Kathihar, India, claim he’s an incarnation of Hindu God Hanuman

A newborn baby was branded an ‘alien’ and later shunned by his mother after being born with an extremely rare condition, this week.

Khalida Begum, 35, gave birth to the as-yet-to-be-named baby on Monday night and was ‘shocked’ when she saw he had a small head and bulging eyes.

Doctors in India provisionally diagnosed him with an extremely rare genetic condition called Harlequin Ichthyosis, which gives sufferers thick skin and deformed features.

However, his symptoms also appear to be consistent with another uncommon defect called Anencephaly.

According to the Centres for Disease Control and Prevention, that causes babies to be born without top parts of the brain and skull. Specifically, the forebrain and cerebrum.

Meanwhile, the remaining parts are often not covered by bone or skin.

Roughly three pregnancies in every 10,000 are affected by anencephaly, while only five UK children are born annually with Harlequin Ichthyosis.

The mother-of-four, from Kathihar in the North Indian state of Bihar, initially demanded midwives remove him from sight. 

‘Several body parts of the baby is not completely developed,’ she told local reporters.  ‘When I saw the baby after delivery for the first time, I was completely shocked to see the alien-looking boy.

‘I couldn’t believe that I had a delivered an alien-like boy. I was so shocked and saddened by this that I asked the midwife to take the baby out of my sight.’

Fortunately, several hours later, she relented and happily began nursing the child. 

Since then villagers have been flocking to the family home, believing he is an incarnation of Hindu monkey God Hanuman. 

The news comes just 24 hours after a 21 year-old man was deemed a deity after a mystery condition left him just 23 inches tall.

Manpreet Singh is the same height and weight as a six month old baby and is believed to be one of the smallest people in the world.

Currently undiagnosed, his condition remains a mystery. But now locals in Punjab, India, consider him a Hindu God reincarnated and visit him daily to be ‘blessed’. 


Harlequin Ichthyosis is extremely rare, and comes out of the blue.

The parents of an affected baby are carriers and will have a one in four risk of any baby being affected.

The condition causes the skin to grow seven times faster than normal.

The skin appears tight, with thick plates of hard scales resembling armour plating or the harlequin suit of a jester.

The skin splits at several areas causing deep cracks. And a sufferer’s face looks stretched with turned out lips and eyelids, and the ears, hands and feet may be hidden by scales.

The extra skin needs to be removed constantly and ointment is also applied four or five times-a-day.

Children who survive will need ongoing intensive skin treatment with creams and courses of retinoid medicine and many require physiotherapy and counselling.

Source: The Ichthyosis Support Group 

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