Scalp ear nipple syndrome

Also Known As:

Finlay-Marks Syndrome; Hereditary syndrome of lumpy scalp, odd ears and rudimentary nipples; Scalp-Ear-Nipple Syndrome

Networked: 3 relevant articles (0 outcomes, 0 trials/studies)

1.	Myopia
2.	Ectodermal Dysplasia (Aplasia Cutis Congenita)
3.	Amastia
4.	Benign Familial Hematuria

Drugs and Important Biological Agents (IBA) related to Scalp ear nipple syndrome:

1.	Potassium Channels (Potassium Channel)IBA 10/01/2021 - "Scalp-Ear-Nipple syndrome: first report of a Potassium channel tetramerization domain-containing 1 in-frame insertion and review of the literature." 10/01/2021 - "Pathogenic missense variants in the potassium channel tetramerization domain-containing 1 (KCTD1) gene are associated with autosomal dominant Scalp-Ear-Nipple syndrome (SENS), a type of ectodermal dysplasia characterized by aplasia cutis congenita of the scalp, hairless posterior scalp nodules, absent or rudimentary nipples, breast aplasia and external ear anomalies. "
2.	CollagenIBA 01/01/2023 - "KCTD1 and Scalp-Ear-Nipple ('Finlay-Marks') syndrome may be associated with myopia and Thin basement membrane nephropathy through an effect on the collagen IV α3 and α4 chains."

1.	Mammaplasty (Breast Reconstruction) 07/01/2021 - "Breast reconstruction via fat grafting for a patient with bilateral congenital amastia (Finlay-Marks syndrome)."