Pachyonychia Congenita
A group of inherited ectodermal dysplasias whose most prominent clinical feature is hypertrophic nail dystrophy resulting in PACHYONYCHIA. Several specific subtypes of pachyonychia congenita have been associated with mutations in genes that encode KERATINS.
Year introduced: 2007
PubMed search builder options
Subheadings:
Tree Number(s): C16.131.077.350.856, C16.131.831.350.856, C16.320.850.250.856, C17.800.529.594, C17.800.804.350.856, C17.800.827.250.856
MeSH Unique ID: D053549
Entry Terms:
- Pachyonychia Congenita Syndrome
- Congenital Pachyonychia
- Pachyonychia, Congenital
- Pachyonychia Congenita, Type 1
- Jadassohn-Lewandowsky Syndrome
- Jadassohn Lewandowsky Syndrome
- Jadassohn-Lewandowski Syndrome (Pc-1)
- Jadassohn Lewandowski Syndrome (Pc 1)
- Syndrome, Jadassohn-Lewandowski (Pc-1)
- Type 1 Pachyonychia Congenita
- Pachyonychia Congenita Type 1
- Pachyonychia Congenita, Jadassohn-Lewandowsky Type
- Pachyonychia Congenita, Jadassohn Lewandowsky Type
- Pachyonychia Congenita Tarda, Type 1
- Pachyonychia Congenita, Type 2
- Jackson-Lawler Syndrome (Pc-2)
- Jackson Lawler Syndrome (Pc 2)
- Syndrome, Jackson-Lawler (Pc-2)
- Type 2 Pachyonychia Congenita
- Pachyonychia Congenita Jackson Lawler Type
- Pachyonychia Congenita, Jackson-Lawler Type
- Pachyonychia Congenita, Jackson Lawler Type
- Jackson-Lawler Type Pachyonychia Congenita
- Jackson Lawler Type Pachyonychia Congenita
Previous Indexing:
See Also: