Display Settings:

Format

Send to:

Choose Destination

Results: 2

1.

Incontinentia pigmenti syndrome

Incontinentia pigmenti (IP) is a disorder that affects the skin, hair, teeth, nails, eyes, and central nervous system. Characteristic skin lesions evolve through four stages: I. blistering (birth to age ~4 months); II. a wart-like rash (for several months); III. swirling macular hyperpigmentation (age ~6 months into adulthood); and IV. linear hypopigmentation. Alopecia, hypodontia, abnormal tooth shape, and dystrophic nails are observed. Neovascularization of the retina, present in some individuals, predisposes to retinal detachment. Neurologic findings including cognitive delays/intellectual disability are occasionally seen. [from GeneReviews]

MedGen UID:
7049
Concept ID:
C0021171
Congenital Abnormality
2.

Incontinentia pigmenti, familial male-lethal type

MedGen UID:
443905
Concept ID:
C2930820
Disease or Syndrome

Supplemental Content

Find related data

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...