Background: The short anagen syndrome (SAS) is a rare idiopathic pediatric disorder characterized by the short duration of the anagen phase. SAS mainly affects Caucasian children. Parents complain of their child's inability to grow long hair. Topical minoxidil may be an effective treatment for SAS; however, a slow spontaneous improvement is typical. Objective: Our aim was to collect data on out cases of SAS and create an algorithm to facilitate diagnosis of SAS. Methods: A retrospective review of 25 patients with SAS was performed within the Dermatology Department of the University of Bologna. We collected data regarding symptoms, pull test, hair card test, trichoscopy, trichogram, treatments, including biotin and minoxidil, and c...
This bachelor thesis is focused on idiopathic short stature. Idiopathic short stature can be found a...
Introduction: Aggrecanopathies are rare disorders associated with idiopathic short stature. They are...
Graham-Little syndrome, also known as Graham Little-Piccardi-Lassueur Syndrome is characterized by t...
Background: The short anagen syndrome (SAS) is a rare idiopathic pediatric disorder characterized b...
Short anagen syndrome is a relatively recently described entity. This syndrome is an unusual conditi...
none3noShort anagen syndrome (SAS) is a recently described disease, but is rarely reported in the li...
BACKGROUND/OBJECTIVES: Loose anagen syndrome (LAS) is a disorder of abnormal anchorage of the hair t...
Loose anagen syndrome (LAS) is a hair disorder involving insufficient anchoring of the hair follicle...
Background and Objectives: Diagnostic delay is common in attenuated Mucopolysaccharidosis Type I (MP...
Loose anagen hair syndrome (LAHS) is characterized by easily extractable anagen hairs that lose the ...
delineation and natural history The sixth reported case of the SHORT syndrome is described and is co...
A 24-year-old boy applied for his nevuses. On dermatological examination, he was noticed to have gli...
SHOX haploinsufficiency is associated with a wide spectrum of conditions, all characterized growth...
Noonan, Turner, and Prader-Willi syndromes are classical genetic disorders that are marked by short ...
IMPORTANCE: Uncombable hair syndrome (UHS) is a rare hair shaft anomaly that manifests during infanc...
This bachelor thesis is focused on idiopathic short stature. Idiopathic short stature can be found a...
Introduction: Aggrecanopathies are rare disorders associated with idiopathic short stature. They are...
Graham-Little syndrome, also known as Graham Little-Piccardi-Lassueur Syndrome is characterized by t...
Background: The short anagen syndrome (SAS) is a rare idiopathic pediatric disorder characterized b...
Short anagen syndrome is a relatively recently described entity. This syndrome is an unusual conditi...
none3noShort anagen syndrome (SAS) is a recently described disease, but is rarely reported in the li...
BACKGROUND/OBJECTIVES: Loose anagen syndrome (LAS) is a disorder of abnormal anchorage of the hair t...
Loose anagen syndrome (LAS) is a hair disorder involving insufficient anchoring of the hair follicle...
Background and Objectives: Diagnostic delay is common in attenuated Mucopolysaccharidosis Type I (MP...
Loose anagen hair syndrome (LAHS) is characterized by easily extractable anagen hairs that lose the ...
delineation and natural history The sixth reported case of the SHORT syndrome is described and is co...
A 24-year-old boy applied for his nevuses. On dermatological examination, he was noticed to have gli...
SHOX haploinsufficiency is associated with a wide spectrum of conditions, all characterized growth...
Noonan, Turner, and Prader-Willi syndromes are classical genetic disorders that are marked by short ...
IMPORTANCE: Uncombable hair syndrome (UHS) is a rare hair shaft anomaly that manifests during infanc...
This bachelor thesis is focused on idiopathic short stature. Idiopathic short stature can be found a...
Introduction: Aggrecanopathies are rare disorders associated with idiopathic short stature. They are...
Graham-Little syndrome, also known as Graham Little-Piccardi-Lassueur Syndrome is characterized by t...