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18q deletion syndrome

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  #1  
Old 9th August 2012, 07:29 PM
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Default 18q deletion syndrome

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Tried searching in PA no luck. Any advice appreciated, mark


CC: A 28 y/o white male with a medical history of "18q deletion syndrome" (generalised decreased joint stiffness).
No symptoms were able to be elicited from the patient, nor the two carers who accompanied the patient, nor the mother.

HPI: Carers report the patient refuses to wear the OTC foot orthoses prescribed to him by a local priivate podiatrist. The patient prefers slippers.

PMH: No other medical history forthcoming.

PE: The patient would not fully cooperate with any examination attempts.
Most of the time in stance he had bilateral externally rotated hip, slightly flexed knees and pes cavus. Occasionally he would extend his knees into genu recurvatum. His left foot had an obvious abducted forefoot.

Gait examination: Bilateral high knee lift with both feet contacting the surface in a midfoot position.

Neurological: unable to assess
Dermatological:WNL
Vascular: unable to assess

Diagnosis:

1. 18q deletion syndrome
2. ?

Treatment Plan:
1. Nothing till advice from more knowledgeable clinicians is received.
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  #2  
Old 9th August 2012, 09:13 PM
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Default Re: 18q deletion syndrome

Quote:
As mentioned above, distal 18q- is associated with an increased incidence of clubfoot and rocker bottom feet. There is also a significant chance of developing pes planus or pes cavus. People with distal 18q- frequently have overlapping toes. Scoliosis and genu varum are also known orthopedic complications in children and adults with distal 18q-.
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Old 9th August 2012, 10:05 PM
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Default Re: 18q deletion syndrome

Thanks Admin. Did you read the, "There is also a significant chance of developing pes planus or pes cavus"
The query is which joint(s) should we increase / decrease which moments?
Which tissue is being stressed beyond the ZOOS, or is in danger of being so in the future?
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Old 10th August 2012, 12:10 AM
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Default Re: 18q deletion syndrome

Mark

I run a monthly clinic looking after kids with del22q11 (DiGeorge/ Velocardiofacial Syndrome).

Like your patient, they are prone to an almost infinite range of orthopaedic and MSK congenital abnormalities, along with just about every other system including serious psychiatric problems.

They are extremely prone to "leg pains".

There is almost no literature on best practice for these patients and those symptoms.

Therefore, in the absence of evidence based options, my advice is to return to first principles and assess and treat as per any other child who would present with these abnormalities. Communication problems abound, so the parent/s are the best source of subjective information.

It's not easy...

LL
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Old 10th August 2012, 07:24 AM
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Default Re: 18q deletion syndrome

Quote:
Originally Posted by markjohconley View Post
Tried searching in PA no luck. Any advice appreciated, mark


CC: A 28 y/o white male with a medical history of "18q deletion syndrome" (generalised decreased joint stiffness).
No symptoms were able to be elicited from the patient, nor the two carers who accompanied the patient, nor the mother.

HPI: Carers report the patient refuses to wear the OTC foot orthoses prescribed to him by a local priivate podiatrist. The patient prefers slippers.

PMH: No other medical history forthcoming.

PE: The patient would not fully cooperate with any examination attempts.
Most of the time in stance he had bilateral externally rotated hip, slightly flexed knees and pes cavus. Occasionally he would extend his knees into genu recurvatum. His left foot had an obvious abducted forefoot.

Gait examination: Bilateral high knee lift with both feet contacting the surface in a midfoot position.

Neurological: unable to assess
Dermatological:WNL
Vascular: unable to assess

Diagnosis:

1. 18q deletion syndrome
2. ?

Treatment Plan:
1. Nothing till advice from more knowledgeable clinicians is received.
Where are the calluses? What does the inside of the slipper look like?

Pes cavus will often cause an equinus. Equinus can cause recruvatum. Pes cavus will often cause high forefoot loads. Without any further information that would make this totally wrong, I would make a soft orthotic from a partial weight bearing foam box impression with a heel lift. That would be after finding out whether the patient would ever wear a shoe that would accommodate the device.

Eric
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Old 10th August 2012, 02:59 PM
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Default Re: 18q deletion syndrome

Thanks Messrs Lisfranc and Fuller.
From what I was told from what she was told slippers are the only footwear of choice at the moment. Calluses and pressure map on sock lining / insole are to be assessed next appt, thanks, mark
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