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Year : 2019  |  Volume : 64  |  Issue : 3  |  Page : 235-238
Naegeli–Franceschetti–Jadassohn syndrome: A rare reticulate pigmentary disorder

Department of Dermatology, SS Institute of Medical Sciences and Research Centre, Davanagere, Karnataka, India

Date of Web Publication20-May-2019

Correspondence Address:
Dr. Manjunath Hulmani
Department of Dermatology, SS Institute of Medical Sciences and Research Centre, Davanagere - 577 005, Karnataka
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/ijd.IJD_653_16

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Naegeli–Franceschetti–Jadassohn syndrome is a rare autosomal dominant form of ectodermal dysplasia affecting sweat glands, nails, teeth, and skin. We report a case of 16-year-old female who had generalized reticulate pigmentation, dental changes, nail changes, and absence of dermatoglyphics and hypohydrosis.

Keywords: Dermatoglyphics, ectodermal dysplasia, KRT 14 gene, Naegeli–Franceschetti–Jadassohn syndrome, reticulate pigmentation

How to cite this article:
Sanodia G, Hulmani M, Kumar V J. Naegeli–Franceschetti–Jadassohn syndrome: A rare reticulate pigmentary disorder. Indian J Dermatol 2019;64:235-8

How to cite this URL:
Sanodia G, Hulmani M, Kumar V J. Naegeli–Franceschetti–Jadassohn syndrome: A rare reticulate pigmentary disorder. Indian J Dermatol [serial online] 2019 [cited 2023 Jun 8];64:235-8. Available from:

   Introduction Top

Naegeli–Franceschetti–Jadassohn (NFJ) syndrome is a rare form of ectodermal dysplasia affecting skin, sweat glands, nails, and teeth. It was first described by Naegeli in 1927, and in 1954, Franceschetti and Jadassohn re-examined the original family and noted the autosomal dominant pattern of inheritance. The incidence is estimated to be one case in 2–4 million population. It is characterized by reticulate hyperpigmentation, ectodermal dysplasia (primarily dental anomalies and hypohidrosis) and hypoplastic dermatoglyphics.

   Case Report Top

A 16-year-old girl born out of a nonconsanguineous marriage presented with complaints of generalized reticulate pigmentation, hypohidrosis, heat intolerance, and nail dystrophy since birth. There was no significant family history. The patient had normal physical, social, and mental development.

On dermatological examination, the patient had reticulate hyperpigmentation involving the whole body and hair showed mild pigmentary dilution with patchy brown discoloration. Reticulate pigmentation was especially more over the neck [Figure 1], chest, both hands and legs. The generalized xerosis of skin was noted.
Figure 1: Reticulate pigmentation over the face and neck

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Dorsal aspect of tongue exhibited diffuse pigmentation [Figure 2]. Teeth showed yellowish discoloration, abnormal dentition, and enamel defects. There was fusiform swelling at proximal interphalangeal joints and flexion at the distal interphalangeal joints. The absence of dermatoglyphics was noted over all the fingers [Figure 3]. Dystrophy of toenails was observed [Figure 4]. General and systemic examination was normal. Complete hemogram, random blood sugar, liver function test, renal function test, and urine analysis were within normal limits. A biopsy specimen taken from the left side of the neck showed basket wave pattern hyperkeratosis with diffuse pigmentation of basal layer. Upper dermis showed pigment incontinence [Figure 5].
Figure 2: Diffuse pigmentation over dorsal aspect of tongue and yellowish discoloration of teeth

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Figure 3: The absence of dermatoglyphics and fusiform swelling of proximal interphalangeal joints and flexion of distal interphalangeal joints

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Figure 4: Toenails dystrophy

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Figure 5: Histopathology: Upper dermis showing pigment incontinence (H and E, ×40)

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   Discussion Top

NFJ syndrome (MIM 161,000) is a rare autosomal dominant form of ectodermal dysplasia that affects the skin, sweat glands, nails, hair, and teeth.[1] The syndrome is allelic to dermatopathia pigmentosa reticularis (DPR) (MIM 125595) due to dominant mutations in the nonhelical E1/V1 domains of keratin 14.[2] The main symptoms and signs are hypohidrosis with diminished sweat gland function and discomfort provoked by heat, lack of dermatoglyphics (fingerprint lines); and reticulate pigmentation of the neck, chest, and abdomen.[3] All the above findings were documented in our case with the involvement of proximal and distal interphalangeal joint which is a unique feature.

Several mutations in the KRT14 gene have been found to cause NFJS/DPR. The KRT14 gene provides instructions for making a protein called keratin 14 which is specifically produced in cells called keratinocytes. The KRT14 gene mutations that cause NFJS/DPR reduce the amount of functional keratin 14 in keratinocytes. A shortage of this protein makes these cells more likely to undergo apoptosis.[4] Due to loss of keratinocytes, there is an alteration in normal development of ectodermal tissues including skin, hair, nails, teeth, and sweat glands.[5]

Hypohidrosis is the most debilitating aspect of the NFJ syndrome as it can lead to collapse after exercise.[6]

Reticulate hyperpigmentation starts around the age of 2 years without a preceding inflammatory stage. The pigmentation is brown to gray-brown and is localized on the trunk, proximal extremities, axillae, groins, flexures, periocular, and perioral regions. The pigmentation shows a gradual increase during the first 10 years of life, and fading starts around the age of 15 years. Patients with NFJS who are older than 70 years only have minimal or no pigmentation left.[7] Some patients develop bullae on the feet during the newborn period.

Abnormalities of dermatoglyphics are divided into four main categories: ridge aplasia, ridge hypoplasia, ridge dissociation, and ridge off the end. Embryologic development of dermal ridges occurs in conjunction with the eccrine glands, and sweat pores are found on the ridges.[8] Ridge hypoplasia refers to poorly formed dermal ridges while ridge dissociation is characterized by a discontinuous pattern in which dermal ridges are broken into short segments. Ridge hypoplasia and dissociation are the abnormalities that can be seen in NFJS as well as in DPR.[9]

Other cutaneous manifestations are palmoplantar keratoderma (diffuse or punctate) and onychodystrophy (onycholysis, brittle nails, subungual hyperkeratosis, and congenital malalignment of the great toenails. Dental anomalies are common and include abnormally shaped teeth, supernumerary teeth, yellow spotted tooth enamel and early loss of teeth occurs.[10] In our case, it shows all the above features except the presence of palmoplantar keratoderma.

Other genodermatosis associated with generalized reticulate pigmentation is DPR, dyskeratosis congenita (DKC), X-linked reticulate pigmentary disorder, Dowling-Degos disease, and reticulate acropigmentation of Kitamura and Haber's syndrome[11] [Table 1].
Table 1: Differential diagnosis of reticulate hyperpigmentation

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NFJS and DPR syndrome do have overlapping phenotypic features, as both are autosomal dominant ectodermal dysplasia. Both manifest with poorly developed dermatoglyphics, reticulate hyperpigmentation of the skin, hypohidrosis, and heat intolerance. Palmoplantar keratoderma, nail dystrophy, and enamel defects are common in NFJS, whereas diffuse alopecia is only seen in DPR.[12]

Reticulate hyperpigmentation, mucosal leukoplakia, bone marrow dysfunction, cytogenetic instability, and a predisposition to malignancy are characteristic of DKC.[10]

The distribution of the reticulate pigmentation in Dowling-Degos disease, dyschromatosis symmetrica hereditaria, and reticulate acropigmentation of Kitamura makes these disorders easy to distinguish.[13]

The x-linked reticulate pigmentary disorder often presents with hypohidrosis and dental anomalies as well as reticulate hyperpigmentation, but additional systemic manifestations as well as the inheritance pattern distinguish it from NFJ.

Histologically, the hyperpigmented skin demonstrates pigment incontinence and melanophages. No specific treatment exists for NFJS, except for symptomatic management of some of the associated conditions. Genetic counseling should be offered to affected individuals planning future children.

Our case contributes to the further understanding of this rare condition. In addition, we were unable to find any previous reports of NFJ syndrome involving the proximal and distal interphalangeal joint.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form, the patient has given her consent for her images and other clinical information to be reported in the journal. The patient understands that name and initials will not be published and due efforts will be made to conceal identity, but anonymity cannot be guaranteed.

Financial support and sponsorship


Conflicts of interest

There are no conflicts of interest.

   References Top

Lugassy J, Itin P, Ishida-Yamamoto A, Holland K, Huson S, Geiger D, et al. Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: Two allelic ectodermal dysplasias caused by dominant mutations in KRT14. Am J Hum Genet 2006;79:724-30.  Back to cited text no. 1
Itin PH, Lautenschlager S. Genodermatosis with reticulate, patchy and mottled pigmentation of the neck – A clue to rare dermatologic disorders. Dermatology 1998;197:281-90.  Back to cited text no. 2
Tubaigy SM, Hassan HM. Naegeli-Franceschetti-jadassohn syndrome in a Saudi Arabian family. J Forensic Sci 2014;59:555-8.  Back to cited text no. 3
Hesse M, Zimek A, Weber K, Magin TM. Comprehensive analysis of keratin gene clusters in humans and rodents. Eur J Cell Biol 2004;83:19-26.  Back to cited text no. 4
Shah BJ, Jagati AK, Gupta NP, Dhamale SS. Naegeli-franceschetti-jadassohn syndrome: A rare case. Indian Dermatol Online J 2015;6:403-6.  Back to cited text no. 5
[PUBMED]  [Full text]  
Whittock NV, Coleman CM, McLean WH, Ashton GH, Acland KM, Eady RA, et al. The gene for Naegeli-Franceschetti-Jadassohn syndrome maps to 17q21. J Invest Dermatol 2000;115:694-8.  Back to cited text no. 6
Itin PH, Burger B. Spontaneous fading of reticular pigmentation in naegeli-Franceschetti-Jadassohn syndrome. Dermatology 2010;221:135-6.  Back to cited text no. 7
Dereure O. Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis. Two allelic ectodermal dysplasias related to mutations of dominant gene coding for keratin 14. Ann Dermatol Venereol 2007;134:595.  Back to cited text no. 8
Shanker V, Gupta M. Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder. Indian Dermatol Online J 2013;4:40-2.  Back to cited text no. 9
[PUBMED]  [Full text]  
Chang MW. Disorders of hyperpigmentation. In: Bolognia JL, Jorizzo JL, Schaffer JV, editors. Dermatology. 3rd ed. Atlanta: Saunders; 2012. p. 1068.  Back to cited text no. 10
Schnur RE, Heymann WR. Reticulate hyperpigmentation. Semin Cutan Med Surg 1997;16:72-80.  Back to cited text no. 11
Al Saif F. Dermatopathia pigmentosa reticularis: Report of a new cases and literature review. Indian J Dermatol 2016;61:468.  Back to cited text no. 12
[PUBMED]  [Full text]  
Franceschetti A, Jadassohn W. On incontinentia pigmenti and differentiation of two syndromes appearing under the same name. Dermatologica 1954;108:1-28.  Back to cited text no. 13


  [Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5]

  [Table 1]

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