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Achondroplasia

General Information about Achondroplasia

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Achondroplasia is a disorder of bone growth. Achondroplasia literally means "without cartilage formation". The problem in this condition is converting the cartilage into bones, particularly the long bones. Achondroplasia is a genetic (inherited) condition that results in abnormally short stature. All persons with achondroplasia are little people. The average height of an adult with achondroplasia is 131 cm (52 inches, or 4 foot 4) in males and 124 cm (49 inches, or 4 foot 1) in females

Achondroplasia is one of the oldest known birth defects. An average figure worldwide is approximately 1 in 25,000 births..
Achondroplasia child
Child with Achondroplasia


Achondroplasia

Short limbs & Lordo-scoliotic Spine


Achondroplasia

Large Head & Faces


Achondroplasia

Typical Hands

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Posted by:  KIA28SINGLE(Guest)  Posted on: 02/08/2012
I HAVE A 4 YEAR OLD LITLE PERSON AND HE GET AROUND PRETTY GOOD TO BE A LITTLE PERSON BUT HE IS OLDER AND WANT TO DO MORE THINGS FOR HISSELF LIKE WIPE HIS BEHINE HOW DO I TEACH HIM HOW TO DO THOSE THINGS



Posted by:  pet35  Posted on: 02/06/2012
gd day, im peter frm nigeria, my baby is diagonised of achondroplasia by a doc in lagos teaching hospital, idi araba. she is a yr old. pls what can i do at least to increase her height.



Posted by:  LeonKwang94(Guest)  Posted on: 01/14/2012
Hi

My is 17 in normal stream of education. He seemed fine but has a painful calf whenever he walks. He has hydrocephalus too. He is now wanting to get help in learning to drive. However I have no means to support that. Any advise will be helpful.
He is bow leg but presumably if you ask your doctor for advise about correcting they will direct you to the appropriate surgeon. The other is stretching leg while she is resting. My son is not too concern whereby I did not seek any help in the area.



Posted by:  anikamways(Guest)  Posted on: 10/21/2011
can anyone please get to know me about fee structure regarding bow leg correction treatment... pleae...



Posted by:  pankajmadan  Posted on: 02/01/2011
I stay in Gurgaon, India. My daughter was diagnosed of achondroplasia just 10 days before her birth. She is 3.5 years old now and goes to school-playgroup and thoroughly enjoys it. We plan to continue her normal education. Though there are no immediate concerns except the height factor, we realize that we should be providing her with some tools and equipments, that make her independent and facilitate her in leading a normal life. For example – a] something that continuously strengthens her knee, b) somethings that helps her manage her basic hygiene requirements, c) somethings that helps her in the bathroom/kitchen, d) somethings that help her with the electric switches, e) somethings that help her climbing stairs and f) any other tool/equipment which would have come in handy to anyone in the group. I would really appreciate if anyone can share their experiences with these. I am happy to share my specific experiences, if required. Regards, Pankaj


Posted by:  Vaman  Posted on: 07/22/2011
Hi Pankaj, I am from Greater Noida and my was son daignosed with achondroplasia in 8th month. He is 5 now and goes to school. Would like to share expirence and any other information which would be helpful for our kids.



Posted by:  pankajmadan  Posted on: 07/26/2011
Hi Vaman, I think we should surely get in touch and share some experience/information. My mail id is pankajmadan76@yahoo.com. Regards, Pankaj



Posted by:  Ayesha82  Posted on: 08/16/2011
hello. i also had the same situation like your, that i got to know abt my son s disorder in last week.my son is 1.5 years old now..but still he can not able to sit by himself...he is using brace to support his back, but still he can not sit...please do tell me your daughter s growth chart...thank u ..




Posted by:  surajgupte  Posted on: 06/29/2010
A very fine article on achondrplasia. Nevertheless,I would have preferred a greater supplementation with clinical photographs and radiographs for driving home the important aspects of this common proble.
If desired, I can share some of the clinical pictures with your readers please.
Dr (Prof) Suraj Gupte, MD, FIAP



Posted by:  vicky09(Guest)  Posted on: 05/24/2010
Hi,

I'm Virginia and i have a 11 month old baby who has been diagnosed with Achondroplasia. My husband is also a dwarf, but I love my family. It is complicated to have baby with Achondroplasia, however I have overcome my fears and have cared for him over a year now. My baby is very handsome, and we have got involved in a club and LPA. Kindly comment if you too would like to join.



Posted by:  dwarf10(Guest)  Posted on: 04/21/2010
ha ha


Posted by:  guest  Posted on: 05/24/2010
If u are luaghing u shouldnt cause its a serious condition and my mom has it. It's very hard to live with without people laughing.




Posted by:  Molly21(Guest)  Posted on: 03/21/2010
Hi,

I was diagnosed with ahondroplasia when I was five weeks old. On Tuseday 23rd March 2010, I am doing a presentation on this. By Tuesday please.
Thanks



Posted by:  Georgedarshana(Guest)  Posted on: 03/05/2010
Hello dear all,
I am George Darshana from Sri Lanka. I have read all your kind comments.My younger daugther who is 4 yrs and in perfect condition, but dr's identified as Achondroplasia. Yes we can see her height and all others are normal. Thank god. I am glad to hear about Tanay's and Laureens' comments. I will surely contact these two dr's. I am now searching how we could make my child as a normal child by leangthening her limbs or if any pharmaceutical treatments are available.I would be grateful if someone can help me to find these contact details. May god bless you.


Posted by:  Molly21(Guest)  Posted on: 03/21/2010
Hi,

I am 12 yaers old and 7 months ago I got offerd limb lengthing and I turned it down. I am from England and would have been in a wheelchair for 6 months if I had had this done.

Thanks

Molls



Posted by:  chunsiew100(Guest)  Posted on: 02/06/2012
Do you have any painful spells on your legs. My son 17 years of age is suffering with pain. He is Essex, England.



Posted by:  n.moolla  Posted on: 01/05/2011
Hi.im from South Africa.my daughter who is now 5 years old was diagnosed with acondroplasia at the 1 year of age.goin to a normal school and coping very well.a FIGHTER TOO!gets some ear aches,but not so often as 3 years ago.can anyone help me with what sought of treatment they have tried that worked?can i get some feedback if stemcell treatment is effective?



Posted by:  mellisadnea  Posted on: 02/25/2011
Heyy i am doing a project on gentic disordiers and i picked achondroplasia, It has moved me in soo many ways. If you would please inboxx me If you would like to come to my school and talk about it i would very muchly apprishate it..




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