Nail-patella syndrome: Difference between revisions
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{{SI}} | {{SI}} | ||
{{CMG}}{{AE}} {{AN}} | {{CMG}} {{AE}} {{AN}} | ||
{{SK}}Iliac Horn syndrome; hereditary osteoonychodysplasia; Fong disease; Turner-Kiser syndrome | {{SK}}Iliac Horn syndrome; hereditary osteoonychodysplasia; Fong disease; Turner-Kiser syndrome | ||
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==== Extremities ==== | ==== Extremities ==== | ||
*Patellar [[apalsia]] | *Patellar [[apalsia]] may be seen | ||
*Unstable knees from patellar subluxation | *Unstable knees from patellar subluxation | ||
*Limited range of motion of [[elbow]] joint | *Limited range of motion of [[elbow]] joint | ||
Latest revision as of 17:11, 17 August 2012
| Nail-patella syndrome | ||
 | ||
|---|---|---|
| Nail of a patient the nail-patella syndrome | ||
| ICD-10 | Q87.2 | |
| ICD-9 | 756.89 | |
| OMIM | 161200 | |
| DiseasesDB | 8773 | |
| MeSH | C05.550.629 | |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Aarti Narayan, M.B.B.S [2]
Synonyms and keywords:Iliac Horn syndrome; hereditary osteoonychodysplasia; Fong disease; Turner-Kiser syndrome
Overview
Nail-patella syndrome (NPS) is a genetic disorder that results in small, poorly developed nails and kneecaps, but can also affect many other areas of the body, such as the elbows, chest, and hips. The name "nail-patella" can be very misleading because the syndrome often affects many other areas of the body, including even the production of certain proteins.[1]:666 It is also referred to as iliac horn syndrome, hereditary onychoosteodysplasia, Fong disease or Turner–Kieser syndrome.[2].
Historical Perspective
Chatelain first described the syndrome in 1820, and its genetics was first documented by Little in 1897.
Pathophysiology
Genetics
The Nail-Patella syndrome is inherited via autosomal dominancy (see autosomal dominant) linked to aberrancy on human chromosome 9's q arm (q stands for longer arm), 9q34. This autosomal dominancy means that only a single copy, instead of both, is sufficient for disorder to be expressed in the offspring, meaning that the chance of getting the disorder from an affected parent is 50%. The frequency of the occurrence is 1/50,000. The disorder is linked to the ABO blood group locus.
Differentiating Nail-patella syndrome from Other Diseases
Epidemiology and Demographics
The prevalence of nail-patella syndrome is estimated to be 1 in 50,000 individuals.
Diagnosis
Symptoms
- Poorly developed fingernails, toenails, and patellae (kneecaps).
- The nails may be absent, pitted, rigged, discolored or a small piece of a thumbnail may be found on the edge of the thumb. The area at the base of the nail is triangular instead of usual crescent shape.
- Elbow deformities
- Some patients are unable to keep their elbow extended or keep their palms up with elbow extended
- Abnormally shaped pelvis bone (hip bone) or outgrowths causing no symptoms
- Knee may be small, deformed or absent
- Some research shows that people with NPS are more prone to glaucoma and scoliosis, due to poorly developed spines.
Physical Examination
Appearance of the Patient
- May have pronounced skeletal deformities
Skin
- Nail changes:
- Presentation varies from no thumbnail or small piece of a thumb nail at the edge of the finger to minor pitting or discoloration
Eyes
Extremities
- Patellar apalsia may be seen
- Unstable knees from patellar subluxation
- Limited range of motion of elbow joint
- Arthodysplasia of the elbow joint may be present
- General hyper-extension of the elbow noted
- Exostosis from the iliac bones : pathognomic feature of the syndrome
- Scoliosis
- Scapular apalsia
- Cervical ribs may be present
- Subluxation of radial head
Laboratory Findings
Blood tests
- Raised serum creatinine
- Increased BUN
- Increased serum urea
- Decreased creatinine clearance
Urinalysis
Treatment
- Medical treatment:
- Enalapril plus Losartan can help decrease proteinuria
- No treatment is available for the dermatological manifestations of the disease
- Surgical treatment:
- Orthopedic correction for knee deformities
References
See also
External links
Template:Phakomatoses and other congenital malformations not elsewhere classified