Acrocraniofacial dysostosis
(Redirected from Kaplan Plauchu Fitch syndrome)
| Acrocraniofacial dysostosis | |
|---|---|
| Other names | Kaplan Plauchu Fitch syndrome |
 | |
| Specialty | Medical genetics |
| Usual onset | Conception |
| Duration | Lifelong |
| Causes | Autosomal recessive inheritance |
| Diagnostic method | Radiography |
| Prevention | None |
| Prognosis | Good |
| Frequency | very rare, only 2 cases have been described in medical literature |
| Deaths | - |
Acrocraniofacial dysostosis, also known as Kaplan Plauchu Fitch syndrome is a very rare hereditary disorder which is characterized by cranio-facial dysmorphisms, hearing loss, digital clubbing, and osseous anomalies.[1] Only 2 cases have been described in medical literature.[2]
Description
[edit]The following is a list of the symptoms of the disorder:[3]
Cranio-facial
[edit]- Acrocephaly
- Hypertelorism
- Ptosis
- Proptosis
- Down-slanting palpebral fissures
- High nasal bridge
- Nostril anteversion
- Short philtrum
- Cleft palate
- Micrognathia
- Ear abnormalities
- Preauricular sinus or cyst
Auditory
[edit]Osseous
[edit]- Metatarsus adductus
- First brachymetacarpia
- First brachymetatarsia
- Proximally placed first toes
- Craniosynostosis
- Pectus excavatum
- Partial duplication of the thumb's distal phalanx
- Malleus and incus dysplasia
- Tall lumbar vertebrae associated with increased interpedicular distance
Discovery
[edit]This disorder was first discovered in 1988 by Kaplan et al. when they described two sisters born to consanguineous parents with all the symptoms mentioned above. They suggested this disorder to be inherited in an autosomal recessive fashion.[4]
References
[edit]- ^ RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Acrocraniofacial dysostosis". www.orpha.net. Archived from the original on 2020-09-28. Retrieved 2022-06-07.
{{cite web}}: CS1 maint: numeric names: authors list (link) - ^ "OMIM Entry - 201050 - ACROCRANIOFACIAL DYSOSTOSIS". omim.org. Retrieved 2022-06-07.
- ^ "Kaplan Plauchu Fitch syndrome - About the Disease - Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov. Archived from the original on 2021-03-18. Retrieved 2022-06-07.
- ^ Kaplan, P.; Plauchu, H.; Fitch, N.; Jéquier, S. (1988-01-01). "A new acro-cranio-facial dysostosis syndrome in sisters". American Journal of Medical Genetics. 29 (1): 95–106. doi:10.1002/ajmg.1320290112. ISSN 0148-7299. PMID 3344780. Archived from the original on 2022-06-07. Retrieved 2022-06-07.