Achondroplasia | |
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At present there is no specific treatment to promote growth in achondroplastics. When special problems complicate achondroplasia, prompt and expert intervention is important. The large opening under the skull should be surgically enlarged in cases of severe narrowing and compression of the spinal cord.The spinal cord compression can require surgery to decompress it. Orthopedic procedures may be required for lengthening of the limb bones and correction of bowed legs. Teeth should be straightened and, if necessary, removed to alleviate the problem. |
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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
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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:
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:
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 .. |
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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. |
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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:
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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