"Nail Abnormalities: Clues to Systemic Disease." Am Family Physician 69.6 Mar. 15, 2004: 1417-1424. Medically Reviewed by a Doctor on 3/30/2017 Next Article [medicinenet.com]

Aging changes in hair and nails (Medical Encyclopedia) Fungal nail infection (Medical Encyclopedia) Ingrown toenail (Medical Encyclopedia) Ingrown toenail removal - discharge (Medical Encyclopedia) Nail abnormalities (Medical Encyclopedia) Nail injuries [icdlist.com]

Indian Dermatol Online J 2015;6:67-74 Subtle nail abnormalities can harbinger appalling systemic diseases. [idoj.in]

There is no other family history of hair or nail abnormalities. On physical examination, the well-developed and well-nourished boy has appropriate behavior for age. [pedsinreview.aappublications.org]

Brachydactyly with short cone-shaped fingers and nail abnormalities, such as koilonychia or pachyonychia, are frequently associated features. [jamanetwork.com]

Abstract Keratosis pilaris is found commonly in isolation as well as associated with other conditions. We describe a family with keratosis pilaris and hereditary koilonychia, with an autosomal dominant pattern of inheritance. [ncbi.nlm.nih.gov]

TY - JOUR T1 - Keratosis pilaris and hereditary koilonychia without monilethrix. [unboundmedicine.com]

[…] extremitatum hereditaria trangrediens et progrediens see Meleda disease Keratosis follicularis (congenital) Keratosis follicularis spinulosa decalvans cum ophiasi Keratosis lichenoides chronica see Lichen ruber moniliformis Keratosis obturans Keratosis [diseasesdatabase.com]

Clinically, this condition manifests in infants as a honeycomblike keratosis of the palms and the soles. It becomes transgredient during childhood. [emedicine.medscape.com]

Kastl IAnton-Lamprecht INielsen P Hereditary palmoplantar keratosis of the Gamborg Nielsen type: clinical and ultrastructural characteristics of a new type of autosomal recessive palmoplantar keratosis. [jamanetwork.com]

Manifestations (A Case Report). 28266357 Tropical Ulcer : Case Report. 28266356 Erythema Multiforme with Depigmentation. 28266355 Estimation of Porphyrins in Cases of Polymorphic Light Eruptions. 28266354 Stevens-Johnson Syndrome : A Study of 17 Cases [nlm.life]