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Living with Apert Syndrome - Aiden Skees' Story

Aiden Skees is a Kentucky boy who was diagnosed with Apert syndrome at birth. Apert syndrome is a genetic birth disorder that causes the bones in his skull, ...

Michael's Apert Syndrome Story

Shortly after Michael's birth, doctors diagnosed him with Apert syndrome, an extremely rare condition that affects about 15 of every 1 million U.S. babies.

Love for Lola (Apert Syndrome)

Lola is diagnosed with Apert syndrome and other children call her weird. She simply wants some friends. Follow SBSK's other socials.

Tinley's David (Apert Syndrome)

Tinley is diagnosed with Apert syndrome and is sometimes teased by other children despite her sweet and bubbly personality. Tinley's brother, who she refers to ...

Apert Syndrome


Apert Syndrome

Professor David Dunaway, Plastic & Reconstructive Surgeon at LCU discusses Apert Syndrome.

Apert Syndrome

Clinical video on Apert Syndrome reviews syndrome and case.

#hopeforhopie amazing transformation Apert syndrome

Hope's transformation after undergoing a Monobloc bipartition midface advancement.

#hopeforhopie amazing transformation apert syndrome

Hope's amazing transformation after undergoing a Monobloc bipartition midface advancement. Apert Syndrome.

Tinley’s Story: Diagnosed at Birth with Apert’s Syndrome (2013)


5-1-2012 Living with Apert Syndrome

VIDOR - by Lindsey Kovacevich - It's called Apert Syndrome. The birth defect is so rare that out of every one million babies born every year no more than about ...

What is Apert's syndrome?


Apert Syndrome baby Joey

This is Joey learning how to sit after 20 long months. Joey was born with Apert Syndrome and has a trach. We are still praying to God that Joey will be able to get ...

What are the causes of Apert syndrome

What are the causes of Apert syndrome - Find out more explanation for : 'What are the causes of Apert syndrome' only from this channel. Information Source: ...

Student With Aperts Syndrome Returns to School


All about Apert's Syndrome

The basics of Apert's Syndrome.

Help Iga -Apert Syndrome


Apert syndrome

Created using PowToon -- Free sign up at http://www.powtoon.com/join -- Create animated videos and animated presentations for free. PowToon is a free tool ...

Cameron Elliott, Apert Syndrome

Join Cameron, family and friends for a 5k on Jan. 20 at Muddy Creek Greenway. Everything begins at 8 a.m. Cameron Elliott has Apert Syndrome. His family and ...

Síndrome de Apert


Fundraiser for girl with Apert Syndrome

A local family is looking to raise money for a girl whose fingers are fused together.

Alaska offers hope for a son stricken with Apert syndrome

For the mother of a boy born with Apert syndrome, going home to Alaska has given her son a chance at a normal life. Read the full story at latimes.com: ...

Apert Syndrome Treatment


Apert syndrome breaking up secretions

This is Joey Kangaroo on Oct 3, 2015 with his chest vest on that vibrates out secretions from his chest. Joey needs this because he isn't mobile yet.

Russian toddler travels to Michigan seeking care for Apert syndrome


Hello Youtube - Unsere Vorstellung

Willkommen auf unserem Kanal! Mein Name ist Olga, ich bin die Mutter von Valerie, einem fröhlichen 4jährigen Mädchen mit Apert Syndrom. Wir möchten ...

Billy and Denise Mitchell. Apert Syndrome.

Billy has a rare condition called Apert Syndrome. A genetic disorder characterised by the premature fusion of certain skull bones. Despite over 50 operations ...

994 Apert's Syndrome


Apert Syndrome

Apert Syndrome.

Apert Syndrome

This video was made for a science project.

Craniofacial Syndromes, Dr. Pat Ricalde

Craniofacial Syndromes: Crouzon Syndrome, Apert Syndrome before and after cranio vault reconstruction.

Zain's Surgerys - Apert Syndrome

Video Made By: Esra Mohammad.


VIDEO FOR CHARITY : 2 Balita Penderita Apert Syndrome di Cilacap, butuh bantuan Segera. Berminat menjadi SAHABAT PENGGALANGAN DANA ?

What Is Apert Syndrome?

In addition, a varied number of fingers and toes are fused together (syndactyly) apert syndrome is form acrocephalosyndactyly, congenital disorder characterized ...

Nothing can hold her back

Meet Angelica Mendoza, an Apert Syndrome Ambassador at BYU-Idaho who is super involved and loves to serve others! She's amazing and absolutely nothing ...

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