| Literature DB >> 31772739 |
Aimé Mbonda Noula1,2, Joel Noutakdie Tochie3.
Abstract
Onychogryphosis is a dermatological disease characterized by hypertrophy, opaque or yellow-brown thickening, gross hyperkeratosis, elongation, and excessive curving of the nail plate, especially that of the big toe of the foot. The resultant nail deformity is often termed "ram's horn nail" or "claw-hand" deformity. Affected patients suffer mainly from pain, and cosmetic concerns. This disorder can be acquired or congenital. Herein, we present the case of an usual form of acquired onychogryphosis affecting all the five nail plates of the left hand in a bit to raise awareness of demaytologist and podiatricians on the occurrence of this a typical form for a timely diagnosis and treament, especially in resource-limited settings where this disease is rare or perhatrps under-diagnosed. We also briefly discuss its diagbosis and management.Entities:
Year: 2019 PMID: 31772739 PMCID: PMC6822601 DOI: 10.1093/omcr/omz100
Source DB: PubMed Journal: Oxf Med Case Reports ISSN: 2053-8855
Figure 1Palmar views (A) before and after surgery (B).
Differences between acquired and congenital onychogryphosis [1]
| Clinical features | Acquired onychogryphosis | Congenital onychogryphosis |
|---|---|---|
| Family history of onychogryphosis | No | Often present |
| History of long-standing poor personal care or neglect or homelessness | Yes | No |
| Age at onset | Adults or elderly people | Present at birth or onset before the age of 1 year or during puberty |
| Affected nails | Affects mainly the great toe | Nails of both hands and feet |
| Associated diseases | Senile dementia, ichthyosis, psoriasis, pemphigus, syphilis, variola, hyperuricemia, varicose veins, stasis dermatitis, ulcers of the lower legs, traumatic injuries to the nails, onychomycosis and thrombophlebitis | Haim–Munk syndrome, palmoplantar hyperkeratosis, severe early-onset periodontitis, pes planus, arachnodactyly, acroosteolysis, Papillon–Lefèvre syndrome, ichthyosis hystrix and ectodermal dysplasia-syndactyly syndrome type I |