<abstract xmlns="http://www.w3.org/1999/xhtml"><p>Netherton syndrome (NS) is a rare genodermatosis characterized by the triad of ichthyosiform erythroderma, hair shaft abnormality and an atopic diathesis. We report a case of a 20-year-old male patient presented with pruritus, decreased sweat secretion and generalized erythema on his body. Netherton syndrome is caused by mutations in the <italic>SPINK5</italic> gene that is a crucial role for epidermal barrier function in the skin. Different clinical and phenotypical features can occur based on various LEKTI-domains mutations. Diagnosis is made by the atopic story, hair shaft abnormality, cutaneous lesions and identification of the <italic>SPINK5</italic> gene mutation. In our patient, we detected a new splice site mutation in the <italic>SPINK5</italic> gene and pili annulati as hair abnormality. Affected patients are usually misdiagnosed because of cutaneous lesions such as atopic dermatitis. Therefore, each clinical finding should be evaluated together. We aimed to present a case with a new <italic>SPINK5</italic> gene mutation and different clinical features in NS.</p></abstract>

Netherton syndrome (NS) is a rare genodermatosis characterized by the triad of ichthyosiform erythroderma, hair shaft abnormality and an atopic diathesis. We report a case of a 20-year-old male patient presented with pruritus, decreased sweat secretion and generalized erythema on his body. Netherton syndrome is caused by mutations in the SPINK5 gene that is a crucial role for epidermal barrier function in the skin. Different clinical and phenotypical features can occur based on various LEKTI-domains mutations. Diagnosis is made by the atopic story, hair shaft abnormality, cutaneous lesions and identification of the SPINK5 gene mutation. In our patient, we detected a new splice site mutation in the SPINK5 gene and pili annulati as hair abnormality. Affected patients are usually misdiagnosed because of cutaneous lesions such as atopic dermatitis. Therefore, each clinical finding should be evaluated together. We aimed to present a case with a new SPINK5 gene mutation and different clinical features in NS.


<div xmlns="http://www.w3.org/1999/xhtml"><sec id="j_bjmg-2020-0012_s_001_w2aab3b7c39b1b6b1ab1aAa"><div>Introduction</div><p>Netherton syndrome (NS) is a rare autosomal recessive genodermatosis of cornification characterized by the triad of congenital ichthyosiform erythroderma/ichthyosis linearis circumflexa, trichorrhexis invaginata (bamboo hair), and an atopic diathesis [<a ref-type="bibr" href="#j_bjmg-2020-0012_ref_001_w2aab3b7c39b1b6b1ab2b1b1Aa">1</a>]. Netherton syndrome was clinically described in 1964 by Wilkinson <italic>et al</italic>. [<a ref-type="bibr" href="#j_bjmg-2020-0012_ref_002_w2aab3b7c39b1b6b1ab2b1b2Aa">2</a>] and its incidence is estimated per 200,000 live births [<a ref-type="bibr" href="#j_bjmg-2020-0012_ref_003_w2aab3b7c39b1b6b1ab2b1b3Aa">3</a>]. This disease, originates from mutations in the <italic>SPINK5</italic> gene (encoding the protease inhibitor lympho-epithelial Kazal type inhibitor, LEKTI), in a wide range from mild to severe. As a result of deficiency in the LEKTI function, the skin permeability increases and epidermal barrier function decreases. The clinical presentation may be quite different in affected people. The location, type and the size of genetic mutations <italic>(SPINKS)</italic>, may affect the phenotypical findings and clinical presentations [<a ref-type="bibr" href="#j_bjmg-2020-0012_ref_004_w2aab3b7c39b1b6b1ab2b1b4Aa">4</a>,<a ref-type="bibr" href="#j_bjmg-2020-0012_ref_005_w2aab3b7c39b1b6b1ab2b1b5Aa">5</a>]. Here, we aimed to present a case with a new mutation in the <italic>SPINK5</italic> gene, different hair shaft abnormality and different clinical features in NS.</p><p><bold>Clinical Presentation</bold>. A 20-year-old male patient was referred to our department with complaints of pruritus, decreased sweat secretion and generalized erythema on his body. Erythematous lesions have been repeated since birth. He was bom at term and did not have any history of collodion membrane at birth. He did not have a family history for this illness and his parents were cousins. In the following years, hair loss and dental development disorders have been added. Dermatological examination showed generalized erythema, dryness affecting almost all the body surface and desquamation on some body areas, regression on frontal hair-line, loss of eyebrows and eyelash. Scalp hairs could not grow and the hair shaft was short and thin. The presence of a hair shaft abnormality called “pili annulati” was demonstrated by trichogram examination [<a ref-type="fig" href="#j_bjmg-2020-0012_fig_001_w2aab3b7c39b1b6b1ab1ab3Aa">Figure 1(a), 1(b), (c);</a><a ref-type="fig" href="#j_bjmg-2020-0012_fig_002_w2aab3b7c39b1b6b1ab1ab4Aa">Figure 2(a), (b), (c)]</a>. We did not detect any changes in the nails, palms and mucosal surfaces. Serum IgE level was found to be elevated (>2000.0 UI/mL). The patient was a student at a university and his mental development was normal. A skin biopsy was performed on the trunk. The histological examination of the biopsy showed a mild hyperkeratosis, hypergranulosis, acanthosis and a perivascular lymphoplasmocytic infiltrate in the upper dermis. Molecular analysis detected a c.1608-1G>A splice site mutation in the <italic>SPINK5</italic> (NM 001127698.1) gene. The patient was considered to carry NS as a result of molecular analysis, clinical and histopathological findings.</p><figure id="j_bjmg-2020-0012_fig_001_w2aab3b7c39b1b6b1ab1ab3Aa" position="float" fig-type="figure"><h2>Figure 1</h2><figCaption><p><bold>(a), (b), (c)</bold>: There is showed erythema and desquamation on the trunk and face, regression in frontal hair-line, loss of eyebrows and eyelash.</p></figCaption><img xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="graphic/j_bjmg-2020-0012_fig_001.jpg" src="https://sciendo-parsed.s3.eu-central-1.amazonaws.com/647108742b88470fbea14533/j_bjmg-2020-0012_fig_001.jpg?X-Amz-Algorithm=AWS4-HMAC-SHA256&amp;X-Amz-Date=20240717T044425Z&amp;X-Amz-SignedHeaders=host&amp;X-Amz-Expires=18000&amp;X-Amz-Credential=AKIA6AP2G7AKP25APDM2%2F20240717%2Feu-central-1%2Fs3%2Faws4_request&amp;X-Amz-Signature=f8db8e8c4566178434558fc01cc9d6590d359fcd7450dc4ac53fd4e1dce93578" class="mw-100"/></figure><figure id="j_bjmg-2020-0012_fig_002_w2aab3b7c39b1b6b1ab1ab4Aa" position="float" fig-type="figure"><h2>Figure 2</h2><figCaption><p><bold>(a), (b), (c)</bold>: In the hair shaft examination, Pili annulati abnormality. (100X or 200X magnification under light microscobic.)</p></figCaption><img xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="graphic/j_bjmg-2020-0012_fig_002.jpg" src="https://sciendo-parsed.s3.eu-central-1.amazonaws.com/647108742b88470fbea14533/j_bjmg-2020-0012_fig_002.jpg?X-Amz-Algorithm=AWS4-HMAC-SHA256&amp;X-Amz-Date=20240717T044425Z&amp;X-Amz-SignedHeaders=host&amp;X-Amz-Expires=18000&amp;X-Amz-Credential=AKIA6AP2G7AKP25APDM2%2F20240717%2Feu-central-1%2Fs3%2Faws4_request&amp;X-Amz-Signature=44d269149b44994b97bb800fa67e35e4c7cb71cac7d248109eefee2b1f567c42" class="mw-100"/></figure><p><bold>Genetic Analysis</bold>. Clinical exome solution by Sophia Genetics® (Saint-Sulpice, Switzerland) was performed for molecular diagnosis of the patient. For the variant filtering process, we considered only nonsense and missense variants, insertions/deletions, and variants at canonical splice sites, excluding variants with minor allele frequency greater than 0.01 in different public and local resources. The c.1608-1G>A splice site mutation was detected in the <italic>SPINK5</italic> (NM_001127698.1) gene. Moreover, this variation has not been reported in GnomAD, Exac and inhouse databases, but it is listed as a ‘disease causing’ mutation at several <italic>in silico</italic> databases. Parenteral segregation was confirmed with Sanger sequencing. Informed consent was obtained from the patient included in this case report.</p></sec><sec id="j_bjmg-2020-0012_s_002_w2aab3b7c39b1b6b1ab1b1Aa"><div>Discussion</div><p>Netherton syndrome is caused by mutation in serine protease inhibitor, kazal type 5 gene, which is located on the long arm of chromosome 5q32. Lympho-epithelial Kazal type inhibitor (LEKTT) is expressed in epithelium, mucosa, thymus and produced by the <italic>SPINK5</italic> gene. Human tissue kallikreins (KLKs) are expressed in the skin including a serine-proteases family and secreted together with LEKTI. The balance of KLKs and LEKTT, including other serine proteases and their inhibitors, is important for regulation of a skin barrier. If KLKs activities increase in the skin, increased activity may break down a normal epidermal barrier.</p><p>Different clinical manifestation are derived from various LEKTI-domains mutations [<a ref-type="bibr" href="#j_bjmg-2020-0012_ref_004_w2aab3b7c39b1b6b1ab2b1b4Aa">4</a>, <a ref-type="bibr" href="#j_bjmg-2020-0012_ref_005_w2aab3b7c39b1b6b1ab2b1b5Aa">5</a>, <a ref-type="bibr" href="#j_bjmg-2020-0012_ref_006_w2aab3b7c39b1b6b1ab2b1b6Aa">6</a>, <a ref-type="bibr" href="#j_bjmg-2020-0012_ref_007_w2aab3b7c39b1b6b1ab2b1b7Aa">7</a>]. Hence, phenotypic features could be substantially different. Up to now, in patients with NS, 80 different mutations have been defined that are associated with the <italic>SPINK5</italic> gene [<a ref-type="bibr" href="#j_bjmg-2020-0012_ref_008_w2aab3b7c39b1b6b1ab2b1b8Aa">8</a>, <a ref-type="bibr" href="#j_bjmg-2020-0012_ref_009_w2aab3b7c39b1b6b1ab2b1b9Aa">9</a>, <a ref-type="bibr" href="#j_bjmg-2020-0012_ref_010_w2aab3b7c39b1b6b1ab2b1c10Aa">10</a>].</p><p>A large proportion of patients with NS start erythematous lesions at birth or soon after, later develop polycylic patches with double edged scaling called ichthyosis linearis circumflexa and may persist throughout their lives [<a ref-type="bibr" href="#j_bjmg-2020-0012_ref_011_w2aab3b7c39b1b6b1ab2b1c11Aa">11</a>]. In our patient, there were no typical lesions, but there was disseminated ichthyosiform erythema affecting almost all the body surface and desquamation on some body areas.</p><p>Hair shaft abnormalities usually occur later than skin lesions. In affected patients, hair shafts are short, thin and do not grow. Trichorrhexis invaginata (TI) is most commonly seen form and happens to depend on invagination of the distal portion of the hair shaft into the proximal portion. The presence of this shaft abnormality can be demonstrated by trichogram or trichoscopy and provide the most particular clue for diagnosis. Trichorrhexis invaginata is just a supportive finding for diagnosis, but its absence does not rule out a diagnosis, as in our case. Our patient had pili annulati as a hair shaft abnomality. Pili annulati is a rare hair shaft disorder consisting of bright and dark sections. There are abnormal air spaces within the bright bands of hair cortex. In this hair shaft abnormality, the hair cannot grow and fragility is not commonly present. We detected other hair shaft abnormalities such as trichorrhexis nodosa and pili torti excluding TI in the literature research (pubmed database) [<a ref-type="bibr" href="#j_bjmg-2020-0012_ref_012_w2aab3b7c39b1b6b1ab2b1c12Aa">12</a>,<a ref-type="bibr" href="#j_bjmg-2020-0012_ref_013_w2aab3b7c39b1b6b1ab2b1c13Aa">13</a>]. However, we could not find any NS case with pili annulati.</p><p>We know that the <italic>SPINK5</italic> gene is expressed on epithelial surfaces. If there is a deficiency in the function of this gene, the penetration of many allergens will increase and it cannot provide a protective effect against these allergens. As a result, atopic manifestation or disorders (such as atopic dermatitis, asthma, allerjic rhinitis, urticaria, food allergies and increased serum IgE levels) will occur. As a matter of fact, it has been suggested that two-thirds of patients have allergic disorders [<a ref-type="bibr" href="#j_bjmg-2020-0012_ref_014_w2aab3b7c39b1b6b1ab2b1c14Aa">14</a>,<a ref-type="bibr" href="#j_bjmg-2020-0012_ref_015_w2aab3b7c39b1b6b1ab2b1c15Aa">15</a>]. Our patient had a high serum IgE level but did not have any atopic manifestation or food allergy.</p><p>Some patients can have recurrent infections, mentalmotor retardation, metabolic imbalance and intestinal pathologies [<a ref-type="bibr" href="#j_bjmg-2020-0012_ref_010_w2aab3b7c39b1b6b1ab2b1c10Aa">10</a>, <a ref-type="bibr" href="#j_bjmg-2020-0012_ref_016_w2aab3b7c39b1b6b1ab2b1c16Aa">16</a>, <a ref-type="bibr" href="#j_bjmg-2020-0012_ref_017_w2aab3b7c39b1b6b1ab2b1c17Aa">17</a>, <a ref-type="bibr" href="#j_bjmg-2020-0012_ref_018_w2aab3b7c39b1b6b1ab2b1c18Aa">18</a>]. AlthoughNS is a rare disease, some familial cases also have been reported [<a ref-type="bibr" href="#j_bjmg-2020-0012_ref_019_w2aab3b7c39b1b6b1ab2b1c19Aa">19</a>,<a ref-type="bibr" href="#j_bjmg-2020-0012_ref_020_w2aab3b7c39b1b6b1ab2b1c20Aa">20</a>].</p><p>The diagnosis is supported by the presence of finding such allergic or atopic story, hair shaft abnormality, ichthyosiform erythroderma and identification of a germline <italic>SPINK5</italic> mutation by DNA sequencing. Although, various treatment methods such as topical corticosteroids, topical calcineurin inhibitors, topical and systemic retinoids, phototherapy and infliximab are used; there is no cure for NS at this time [<a ref-type="bibr" href="#j_bjmg-2020-0012_ref_011_w2aab3b7c39b1b6b1ab2b1c11Aa">11</a>].</p><p><bold>Conclusions</bold>. As a result, NS can be presented in a manner that can range from mild clinical signs to life-threatening complications, especially in the neonatal period. If we evaluate these clinical presentations alone, we may cause a misdiagnosis or a delayed diagnosis. Therefore, it will be a more accurate approach to evaluate each clinical findings together. We presented a patient with NS who had different clinical features because of the presence of a previously unreported pili annulati abnormality and a new <italic>SPINK5</italic> gene mutation, the absence of mental retardation and frequent infections.</p></sec></div>

A new splice-site mutation of <italic>SPINK5</italic> gene in the Netherton syndrome with different clinical features: A case report

Balkan Journal of Medical Genetics

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

A new splice-site mutation of  gene in the Netherton syndrome with different clinical features: A case report

Netherton syndrome (NS) is a rare genodermatosis characterized by the triad of ichthyosiform erythroderma, hair shaft abnormality and an atopic diathesis. We...

A new splice-site mutation of SPINK5 gene in the Netherton syndrome with different clinical features: A case report

Article Category: Case Report

Publié en ligne: 26 août 2020

Pages: 91 - 94

DOI: https://doi.org/10.2478/bjmg-2020-0012

Mots clés
Hair shaft abnormality, Netherton syndrome (NS), gene mutation

© 2020 Erden E, Ceylan AC, Emre S, published by Sciendo

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

Figure 1

Figure 2

A new splice-site mutation of SPINK5 gene in the Netherton syndrome with different clinical features: A case report

Article Category: Case Report

Publié en ligne: 26 août 2020

Pages: 91 - 94

DOI: https://doi.org/10.2478/bjmg-2020-0012

Mots clésHair shaft abnormality, Netherton syndrome (NS), gene mutation

© 2020 Erden E, Ceylan AC, Emre S, published by Sciendo

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

Figure 1

Figure 2

Mots clés
Hair shaft abnormality, Netherton syndrome (NS), gene mutation