We report a case of Noonan syndrome with loose anagen hair (NS/LAH), a rare variant of Noonan syndrome, with associated trichorrhexis nodosa and trichoptilosis. The SHOC2 mutation may be responsible for these additional hair shaft defects, revealing the importance of microscopic examination of hairs in these patients
Background Noonan and Noonan-like syndromes are multisystem genetic disorders, mainly with autosoma...
Noonan syndrome (NS) is an autosomal dominant disorder consisting of short stature, short and/or web...
Noonan syndrome (NS) is a relatively common, clinically variable and genetically heterogeneous devel...
Noonan-like syndrome with loose anagen hair (NS/LAH; OMIM #607721) has been recently related to the ...
Noonan-like syndrome with loose anagen hair (NS/LAH; OMIM 607721), recently related to the invariant...
Noonan-like syndrome with loose anagen hair (NS/LAH; OMIM 607721), recently related to the invariant...
Noonan-like syndrome with loose anagen hair (NSLH), also known as Mazzanti syndrome, is a RASopathy ...
Noonan-like syndrome with loose anagen hair (NSLH), also known as Mazzanti syndrome, is a RASopathy ...
Moyamoya disease is a unique chronic cerebrovascular condition caused by progressive stenosis of the...
Pathogenic variants in the RASopathy-causing SHOC2 gene have been suggested to cause Noonan syndrome...
Noonan syndrome (NS) is among the most common nonchromosomal disorders affecting development and gro...
Noonan syndrome (NS) is among the most common non-chromosomal disorders affecting development and g...
Noonan syndrome (NS) is an autosomal dominant disorder with vast heterogeneity in clinical and genet...
Noonan syndrome (NS) is a genetic disorder caused by autosomal dominant inheritance and is character...
Loose anagen hair syndrome (LAHS) is an underestimated cause of noncicatricial alopecia among childr...
Background Noonan and Noonan-like syndromes are multisystem genetic disorders, mainly with autosoma...
Noonan syndrome (NS) is an autosomal dominant disorder consisting of short stature, short and/or web...
Noonan syndrome (NS) is a relatively common, clinically variable and genetically heterogeneous devel...
Noonan-like syndrome with loose anagen hair (NS/LAH; OMIM #607721) has been recently related to the ...
Noonan-like syndrome with loose anagen hair (NS/LAH; OMIM 607721), recently related to the invariant...
Noonan-like syndrome with loose anagen hair (NS/LAH; OMIM 607721), recently related to the invariant...
Noonan-like syndrome with loose anagen hair (NSLH), also known as Mazzanti syndrome, is a RASopathy ...
Noonan-like syndrome with loose anagen hair (NSLH), also known as Mazzanti syndrome, is a RASopathy ...
Moyamoya disease is a unique chronic cerebrovascular condition caused by progressive stenosis of the...
Pathogenic variants in the RASopathy-causing SHOC2 gene have been suggested to cause Noonan syndrome...
Noonan syndrome (NS) is among the most common nonchromosomal disorders affecting development and gro...
Noonan syndrome (NS) is among the most common non-chromosomal disorders affecting development and g...
Noonan syndrome (NS) is an autosomal dominant disorder with vast heterogeneity in clinical and genet...
Noonan syndrome (NS) is a genetic disorder caused by autosomal dominant inheritance and is character...
Loose anagen hair syndrome (LAHS) is an underestimated cause of noncicatricial alopecia among childr...
Background Noonan and Noonan-like syndromes are multisystem genetic disorders, mainly with autosoma...
Noonan syndrome (NS) is an autosomal dominant disorder consisting of short stature, short and/or web...
Noonan syndrome (NS) is a relatively common, clinically variable and genetically heterogeneous devel...