Thursday, August 30, 2012

What is Ectrodactyly? An overview.


When I first found out that my baby would be born with ectrodactyly, I was devastated and shocked.  But mostly, I was scared and and uncertain of the future.  A lot of questions wandered around my head.  How bad would my sons hands and feet turn out?  what would they look like?  How did he get this condition?  What would my son's physical limitations be?  What would the doctors be able to do for him? 

Well the way I dealt with this was to do as much research as possible.  Throughout my life, whenever I have faced a major ordeal, I have responded by learning as much as I could about the problem.  'Knowdledge is power' as they say, so I like to face my problems by being well informed.

It turns out that ectrodactyly is rare and kind of hard to find a lot of information on.  If you google "ectrodactyly", you are likely to see a lot of links to medical freak-show type websites, Bree Walker, and complicated scientific research papers on genetics. But I did the best I could and this is what information I could get from different resources.

Ectrodactyly is a Greek word that literally means abortion of a finger.  A different website states that ectrodactyly translates to "monstrous fingers".  The medical definition of ectrodactyly is the congenital loss of fingers or toes.  A more common (and recognizable) nick name for ectrodactyly is "lobster-claw syndrome", as hands or feet affected often take the shape of a claw.  Ectrodactyly has also been known as split-hand or split-foot malformation.  Another more specific scientific term for the condition are the initials 'EEC', which stands for ectrodactyly, ectodermal dysplasia, and facial cleft syndrome, naming three features associated with the condition.

The most typical presentation of ectrodactyly occurs in the hands and/or feet.  It involves the absence of the three middle digits, leaving a large cleft down the middle.  This gives the hand and/or foot a claw-like appearance.  


My son's right hand, which only has two fingers

Ectrodactyly can also occur in other variations.  Sometimes, only one or a couple of digits can be missing, with or without the cleft.  In other cases, hands and/or feet can actually have extra digits or webbing.  (By the way, the presence of an extra digit is known as syndactyly.)


 In the past, doctors have typically tried to repair and close the cleft in attempt to give the hand and/or foot a more normal appearance and a narrower shape.  Now, doctors are realizing that such surgeries might be unnecessary and can actually cause lost of functionality and movement.

For example, my son has two fingers, a thumb and a pinky.  The orthopedic surgeon told us that if they closed the cleft in the middle of his hand, he would lose the opposing thumb.  He would not be able to pick things up or grip things with that hand anymore.  Hand prosthetics are also unnecessary and would only get in the way.  We were told that children are very resilient and learn how to adapt, often times turning their "disability" into amazing abilities :-).

Both of my son's feet are affected by ectrodacyly.  He only has one toe on each foot and his feet are positioned upside down and backwards. Ectrodactyly can cause deformities in other bones, as well.  This is what happened with my baby, as his right femur (thigh bone) is misshapen too.  It is dramatically curved up, causing his knee to be rotated to the side.  The doctor told us that both of his feet will need to be amputated when he is six months old, so that he will be able to learn how to walk on prosthetics by the time he turns one.  At this point, we are not sure how his right femur will be treated. We are waiting for the specialist to tell us if it can be repaired surgically or if that whole leg will just need to be amputated.
my sons legs.  Notice how his right thigh bone is curved up.





Two boys with ectodermal dysplasia
Earlier, I mentioned that Ectrodactyly is sometimes called EEC syndrome for ectrodactyly, ectodermal dysplasia, and facial cleft syndrome.


 Ectodermal dysplasia is the absence of sweat glands causing a variety of skin and pigmentation problems.

 



Cleft palate (a split in the upper part of the lip and mouth) can also be associated with this condition.


A small percentage of people with ectrodactyly also have some level of hearing loss.  Interestingly, I have been partially deaf since birth.  All of my extremities are normal and deafness is my only symptom of ectrodactyly. My father has ectrodactyly and I didn't realize I had inherited it from him until my son was born with it.  I had always thought my hearing loss was a separate random condition.    But apparently, I do have it and I have a 50% chance of giving it to my offspring. 

This brings us to how ectrodactyly happens. It is a very rare condition and only 1 in a 100,000 children are born with it. It is usually a genetically inherited condition, as in one parent passes it down to their child.  However, ectrodactyly has occasionally been known to occur spontaneously even when neither parent has it. Most commonly though, it runs through the entire family and can be traced back for several generations.  It affects families of all ethnicity from all over world, including Asia, the UK, south America, Africa and the US.  Even some animals can have ectrodactyly.

 Well, ectrodactyly does run in my family.  My father has it and  several of his brothers and sisters (my aunts and uncles) have it, as well.  But neither their father or mother (my grandparents) have it and we are not sure of which generation started it.  I am the only child of my father and mother, his first wife. My only symptom of ectrodactyly is the deafness.  My father has ten other children with his second wife and the majority of them are affected to varying degrees.  Most of my half-brothers have it in their feet and several of my half-siblings have hearing loss. One of my brothers was actually affected in the same way as my son and he also had to have both of his legs amputated.

So there you have it. A little information on ectrodacyly and how my little miracle is affected by it. 






  











18 comments:

Ar2CoolWriter said...

Hi,

I would like to introduce myself. My name is Aleshia and both my daughter and I have been affected with ectrodactyly, but no one else in our family that we know of.

My deformities are bilateral, only affecting my left side. My left hand is normal, but the middle and ring finger are webbed together up to the knuckle. My left foot has webbing of the 1st 2 toes, and I have a middle toe, there was a 4th bone..but no toe and it was removed when I was very young, and I have a pinky toe that bulges on the side making it uncomfortable in shoes.

My daughter has EEC. She only has 1 finger total and it is bent downward but she has great functionality with it including eating, picking up the smallest things, lol and stabbing us with it. The nail on her finger is both on top and bottom. Her left side is like a nub. Both her feet only have the 2 toes..both looking different..her left has become extremely wide but doctors dont want to touch her..saying shes too young??

She also cannot be in the sun or heat for long. When she was a baby I took her to the pool a few times and she became lethargic, eyes watered real bad, and she ended up with a fever every time the following day. We discovered she must have hyperhydrosis...lack of sweat glands..but her geneticists didnt seem to really understand when I spoke to her about it..?

My daughter is highly intelligent, so this condition does not affect the cognitive side, just physical.

You may friend me on Facebook if you would like to keep in touch. I have looking for support for both me and my daughter.
http://www.facebook.com/aleshia.green.1

Unknown said...

Thank you so much for writing Aleshia. I love hearing from other mothers who have faced this with their children. I'm sending you a friend request on facebook and you should join the ectrodactyly group on facebook too. There is lots of support there! :-)

Unknown said...

Hi,
First when I saw my son coming out with such conditions.. I almost fented.. but couldn't act wild cse did not want shock my wife.. my son is having both hands and legs with three fingers and three toes with close left ear.. I was blaming my wife for watching aliens movies and ET.. but as a muslim, I had to accept that is a allah giving and creature. . Can't complain neither blame anybody.. just was praying for a good and healthy growth and brain.. now he is almost 3 years.. adam can walk can run lile a crazy and can grab things strangely but he can. Talking not yet start. . Im following and doing check up every mow and then.. please send me the FB page address.. mine is chalghoumi@gmail.com..
Waiting for your kind reply.. regards. Allah bless everyone

Unknown said...

Hi Brahim! I loved your comment so much, I gave it it's own post. check it out up above :-)

Sammi said...

Thank you so much for your post! My brother has ectrodactyly as well and was also born deaf. It has never occurred throughout my family history and my grandmother is a geneologist who has traced our history and still hasn't found out any more information.

dianagraves said...

My sister has it on her right hand only. Her arm is very thin a d short, elbow turned backwards and just a thumb and finger on her hand. She has no other symptoms of EEC, but she's 15 now and she hates herself so much it makes me cry for her. She cuts up her legs...We put her in therapy and it helped but we're in that awful Goldilocks zone where we're too poor to afford it, but not poor enough for help. Do you have any thoughts on how I could help her? It's a VERY sensitive subject for her. She was raised as a child to think of herself as special in a great way, and loved her hand...but high school has taught her differently. :-(

Unknown said...

My name is Matt I'm 27 years old and I have a cleft hand I'm missing a middle finger on my right hand and just to say it sucks if you can put your child in therapy do it because I use to get teased a lot I grown to ignore it but always remembered so them thoughts stuck with me my whole life. Girls either look at it weird and move away or they laugh,I'm still trying to not care what people say but it's hard when you reach for a hand shake they look at you like your an alien.

Unknown said...

Hope your sis is feeling better...i see this is years later to respond. My husband has a similar hand and he is awesome. He can do anything. And our 2 kids don't have it. My email is rflynn@keuka.edu and that's my fb email. Anytime she wants to or you want to talk. Hugs

Unknown said...

Those girls are stupid. My husband has a cleft hand and he is awesome. He rides a motorcycle and can do anything and I'd destroy anybody who bothered him. And the people who say anything....i hint that his hand is even better in private.That shuts them up quick. I know there are hot women who could give a dang about a cleft hand because I'm one of them. Hugs to you!

Unknown said...

Hello, my son has EEC in both hands and feet, and I'm from South Africa, Pretoria. He is now 6 years old and this year he started school. I'm grateful because he's attending a normal school. My only problem is the stigma of other people towards him. I'm looking for other children or people with EEC so that we can form a support group and for my boy to know that he's not the only one who's looking like that. He is the first person with this syndrome both on my side and that of my husband.

lulu said...

Hi..am a South African lady, my granddaughter has it on her hand and feet (lobster feet), she is two months old. We are trying to deal with the condition but its soo hard. Maybe talking to those who are experiencing the same will help a lot. She is so adorable, we are just scared for her when she starts schooling.

Unknown said...

Hi! I don't know if you still check this blog, but my brother has ectrodacyly on his right hand (only a thumb and index finger), along with him missing his pinky on his left hand. It is very hard for him in his own mind to accept why God would allow this, but he neither suffers from deafness, foot deformities, or anything else the ectrodacyly could affect. He is a physically able bodied person on all levels, and socially has lived a normal life, aside from the people that stare, and of course some level of bullying from children. But he is now 18, and has defied what people would think his capabilities should be. I'd say the social aspects of this phenomena are worse than the physical differences themselves. Unless of course it affects their mobility/physical capabilities. But anyways, just some insight...I'm so thankful you made this blog. Haven't seen much of a community for this topic.

lulu said...

Hi Marriam..Havent been checking the post. Am also from South Africa in Pretoria. Am not sure if you are still checking. My granddaughter has just turned 1 year 2 months now. She started walking on 15 July 2018. She is able to use her hands and we have now adjusted to her condition that we find it normal. The only thing worrying her mom is when she has to start schooling. So far we are happy and shes such a gift and very intelligent.

Ahne SD said...

Thank you for sharing this, i wish you well

Second Toe Pain

Unknown said...

hi, i wanna contact you, you are super mom

Unknown said...

My son is 8 months with a cleft hand- missing all middle digits, only has his thumb and pinky fingers. He uses it as if it was meant to be his dominant hand. We had no idea of his hand while I was pregnant. We always saw him with his hand in his mouth- so now we just say he ate his fingers. I feel like we just have to go with it, but I don't want to be insensitive to him as he gets older. We've been told to treat him as any normal kid and don't stop him/help him when he tries to use that hand.
I am afraid of the bullying that he may have to deal with when he gets older. I am afraid of the teasing when he starts school.
Everyone around him loves him, plays with him and doesn't make any sort of "deal" out of it. I am thankful for everyone accepting him and supporting us in the sense that they don't question it or stay away or make weird faces. They are there with us. He has a large group of people who love him and I'm hoping that he will always know he is loved.
To "Tha Real BlackSharkmonkey"... it's been over 2yrs from your original post. How are you now? I can't help but hope people are more understanding and accepting.

Unknown said...

Hi!
I bad a cleft lip and my uncle a cleft lip and palate. We were fortunate. My youngest daughter was born with cleft feet. We are still figuring everything out as she is 7 months old. Her right foot is a complete V. She has 4 toes but only 2 visible as they are fused together. On her left foot the V shape started but thankfully stopped so all that is wrong is the missing of a toe.

She is struggling a little when it comes to putting her feet down as her pinky toe on her V foot curls and doesnt sit flat :(
We visit the specialist in June though! :)

Proud Momma said...

Hello!
My son is almost 5 now and was born with his thumb and pinky on his left hand and only a pinky on his right hand. Both of his feet are v shaped with only two toes on each. We did find this out when I was pregnant but even my doctor didn't know what to think as she had never seen it before. Of course I was worried and had all the questions...how will he do this, how will he do that. My son is AMAZING!! I have never met someone that is more determined that he is. He plays soccer, basketball, baseball, football and does karate. He decided one day he wanted his training wheels off and within two days he was riding his bike without training wheels. There really isn't anything that he can't do. He has asked questions and it does break my heart and I do worry for school and other kids but he has an awesome personality and tons of love and support from a lot of people. So for now we just take it one day at a time and let him know everyday that we love him and he is perfect!

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