Naegeli syndrome in Child
Reticulate hyperpigmentation of the trunk, neck, and axilla often occur within the first 2 years life with gradual resolution into late life. Patients have palmoplantar keratoderma, which, in turn, causes loss of dermatoglyphics. Teeth can have an abnormal shape in addition to enamel defects. Extensive dental work at a young age is often required, and this offers a key diagnostic clue. Nails can be brittle or malaligned. Hair is often normal, which can be a key distinguishing feature from other ectodermal dysplasias.
Hypohidrosis or anhidrosis often manifests as heat intolerance in childhood and is the primary cause of morbidity in this condition.
Q82.4 – Ectodermal dysplasia (anhidrotic)
239084001 – Franceschetti-Jadassohn Syndrome
Differential Diagnosis & Pitfalls
- – Thought to be allelic to Franceschetti-Jadassohn with many similar features but has alopecia, lack of dental anomalies, and stable reticulate hyperpigmentation.
- Weary-Kindler – Shared features include congenital acral bullae, reticulate hyperpigmentation, and development of acral keratoses. Presence of photosensitivity, poikiloderma, and severe periodontal disease are helpful in distinguishing these patients from those with Franceschetti-Jadassohn.
- – Also has reticulate hyperpigmentation with classic 20 nail dystrophy including distal nail plate elevation. Patients will lack hypohidrosis and dental changes.